Minutes of the meeting 8th August 2021
Ref: SMTA/Aug.2021/EBM/MIN-13
Date: 08-08-2021
MINUTES
Pursuant to the Agenda Notice dated 18th July, 2021 the 13th Emergent Executive Body Meeting of The Surgical Manufacturers and Traders Association was held Online by video conferencing on 18th July, 2021 at 05.30 PM.
Following members were present:
1. Mr.PradeepChawla (In the Chair)
2. Mr. Puneet Bhasin
3. Mr.JitenderSareen
4. Mr.SatishMahajan
5. Mr.Anurag Seth
6. Mr.Harpereet Singh
7. Mr.Karan BirSuri
8. Mr.Rajesh Sawhney
9. Mr.RakeshSawhney
10. Mr.Ramesh Bhasin
11. Mr.RakeshArora
12. Mr.Virender K. Suri
13. Mr. R.C.Gupta
14. Mr.S.B. Sawhney
15. Mr. Arun Sharma
16. Mr.RajeshNarula
Absent: Mr. Ashok Makkar, Mr.Ravi Awasthi, Mr.Vijay K Aggarwal & Mr. Ashok Sareen.
Welcome Address by the President:
The President welcomed all the Membersto the Online Executive Body Meeting of the Association and thanked everybody to make it up on the short notice. Thereafter, he requested the Secretary Sh. Puneet Bhasin to start the meeting as per agenda.
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Scheme Guidelines for Remission of Duties and Taxes on Exported Products (RoDTEP)
To be published in the Gazette of India Extraordinary Part II Section 3, Sub Section (II)
Government of India
Ministry of Commerce & Industry
Department of Commerce
Udyog Bhawan, New Delhi
Notification No: 19 /2015-2020
New Delhi, the (17th August, 2021)
Subject: Scheme Guidelines for Remission of Duties and Taxes on Exported Products (RoDTEP)
S.O.(E): In exercise of the powers conferred by Section 5 of the Foreign Trade (Development and Regulation) Act, 1992 read with Para 1.02 of the Foreign Trade Policy 2015-20, the Central Government hereby makes the following amendments in the Foreign Trade Policy 2015-20 with immediate effect:
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APPENDIX 4 R – Notified on 17-08-2021 under Notification No 19/2015-20
APPENDIX 4R : Scheme for Remission of Duties and Taxes on Exported Products (RoDTEP)
| RODTEP
Entry No. |
Tariff Item | Description of Goods (As per CTH ) | RODTEP
Rate as % age of FOB (#) |
UQC | Cap (Rs. Per UQC) |
| (1) | (2) | (3) | (4) | (5) | (6) |
| 0301 | LIVE FISH | ||||
| Ornamental Fish | |||||
| 1 | 03011100 | Freshwater | 0.5% | Kg | |
| 2 | 03011900 | Other | 0.5% | Kg | |
| Other Live Fish | |||||
| 3 | 03019100 | Trout (Salmo trutta, Oncorhynchus mykiss, Oncorhynchus clarki, Oncorhynchus aguabonita, Oncorhynchus gilae, Oncorhynchus apache and Oncorhynchus chrysogaster) | 0.5% | Kg | |
| 4 | 03019200 | Eels (Anguilla spp.) | 0.5% | Kg | |
| 5 | 03019300 | Carp (Cyprinus spp., Carassius spp., Ctenopharyngodon idellus,Hypophthalmichthys spp., Cirrhinus spp., Mylopharyngodon piceus, Catla catla, Labeo spp., Osteochilus hasselti, Leptobarbus hoeveni, Megalobrama spp. | 0.5% | Kg | |
| 6 | 03019400 | Atlantic and PacficBluefin tunas (Thunnus thynnus) | 2.5% | Kg | 16 |
| 7 | 03019500 | Southern bluefin tunas (Thunnus maccoyii) | 2.5% | Kg | 16 |
| 8 | 03019900 | Other | 0.5% | Kg | |
| 0302 | FISH, FRESH OR CHILLED, EXCLUDING FISH FILLETS AND OTHER FISH MEAT OF HEADING 0304 | ||||
| Salmonidae, excluding edible fish offal of sub-headings 0302 91 to 0302 99 | |||||
| 9 | 03021100 | Trout (Salmo trutta, Oncorhynchus mykiss, Oncorhynchus clarki, Oncorhynchus aguabonita, Oncorhynchus gilae, Oncorhynchus apache and Oncorhynchus chrysogaster) | 0.5% | Kg | |
| 10 | 03021300 | Pacific Salmon (Oncorhynchus nerka, Oncorhynchus gorbuscha,Oncorhynchus keta, Oncorhynchus tschawytscha, Oncorhynchus kisutch, Oncorhynchus masou and Oncorhynchus rhodurus) | 0.5% | Kg | |
| 11 | 03021400 | Atlantic salmon (Salmo salar) and Danube salmon (Hucho hucho) | 2.5% | Kg | 16 |
| 12 | 03021900 | Other | 2.5% | Kg | 16 |
| Flat fish (Pleuronectidae, Bothidae, Cynoglossidae, Soleidae, Scophthalmidae and Citharidae) excluding edible fish offal of sub-headings 030291 to 030199: | |||||
| 13 | 03022100 | Halibut (Reinhardtius hippoglossoides, Hippoglossus hippoglossus, Hippoglossus stenolepis) | 2.5% | Kg | 16 |
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Last date for voluntary registration of Manufacturers
30th September, 2021 is last date for voluntary registration of Manufacturers for their Medical Devices made in India at CDSCO https://cdscomdonline.gov.in/NewMedDev/Homepage.
Please register if not done or inform reasons / challenges/ inability for not doing so and help desired.
After 30th September, 2021 Medical Devices that are not registered will not be permissible to manufacture, import or sell in India without prior compulsory registration.
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All the shops & establishments shall remain closed on 14th August 2021
Dear Members,
Due to the Security reasons on the occasion of Independence Day, it is requested that all the shops & establishments shall remain closed on 14th August 2021 in the vicinity of Bhagirath Palace & Chandni Chowk.
Regards
Puneet Bhasin
Secretary -SMTA
- Published in Notifications
Extension in period of modification of IEC
DATE: 9th August 2021
To be published in the Gazette of India Extraordinary Part-II, Section-3, Sub-Section (II)
Government of India
Ministry of Commerce & Industry
Department of Commerce
Directorate General of Foreign Trade
Notification No.16, 2015-2020
New Delhi, Dated: 9th August, 2021
Subject: Extension in period of modification of IEC till 31.08.2021 and waiver of fees for IEC updation done during August, 2021— reg.
S.O.(E): In exercise of powers conferred by Section 3 read with Section 5 of FT (D&R) Act, 1992, read with paragraph 1.02 and 2.01 of the Foreign Trade Policy, 2015-2020, as amended from time to time, the Central Government hereby amends the provision in Para 2.05(d) of Chapter-2 of Foreign Trade Policy, 2015-2020 as under:
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Office Memorandum Dated 30th July 2021
DATE: 30th July 2021
File No.-20(8)/43/2021/Div.VI/NPPA
Government of India
Ministry of Chemicals & Fertilizers
Department of Pharmaceuticals
National Pharmaceutical Pricing Authority
OFFICE MEMORANDUM
The Government vide Gazette Notification No. S.O. 2899(E) dated 20th July 2021 has made an amendment in the Drugs (Prices Control) Order, 2013 by inclusion of Form-VI “Proforma for Price List of Medical Devices”. The same is enclosed for your reference as Annexure-I.
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No. SMTA/JULY-31/Prayer Meeting
No. SMTA/July.31/Prayer Meet
With profound grief & sorrow, we regret to inform the sad demise of our beloved Smt Chander Prabha Sareen W/o Late Sh. Suraj Prakash Sareen on 21st July 2021.
Rasam Pagdi will be held on 31st July 2021, Saturday from 3:00 PM to 4:00 PM at Ashoka Bhawan, Ashoka Niketan, Anand Vihar, Delhi – 110092.
Keeping the pandemic situation in mind, you can join us for the prayer meeting online via Google Meet
Google Meet joining link
https://meet.google.com/wfj-viqc-gsr
In Grief,
Sareen Family
- Published in Condolences
Classification of In-vitro Diagnostic Medical Devices
DATE: 23rd July 2021
Drugs Controller General (India)
Directorate General of Health Services
FDA Bhawan, Kotla Road, New Delhi
NOTICE
File No. IVD/Misc/196/2020
Subject: Classification of In-vitro Diagnostic Medical Devices under the provisions of Medical Devices Rules, 2017 – Regarding.
Safety, quality and performance of Medical Devices and In-vitro Diagnostic Medical Devices are regulated under the provisions of the Drugs and Cosmetics Act, 1940 and rules, made there under. For the regulation of Medical Devices and In-vitro Diagnostic Medical Devices with respect to the import, manufacture, clinical investigation, clinical performance evaluation, sale and distribution, the Central Government, after consultation with the Drugs Technical Advisory Board, has notified Medical Devices Rules, 2017 vide G.S.R. 78(E) dated 31.01.2017 which is already implemented from 01.01.2018.
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Classification of Medical Device pertaining to Dermatological & Plastic Surgery
DATE: 26th July 2021
Drugs Controller General (India)
Directorate General of Health Services
FDA Bhawan, Kotla Road, New Delhi
Notice
File No. 29/Misc./0312020-DC (147)
Subject: Classification of Medical Device pertaining to Dermatological & Plastic Surgery under the provisions of Medical Devices Rules, 2017- Reg.
Safety, quality and performance of medical devices are regulated under the provisions of the Drugs and Cosmetics Act, 1940 and rules made thereunder. For the regulation of medical devices with respect to the import, manufacture, sale and distribution, clinical investigation, the Central Government, after consultation with the Drugs Technical Advisory Board, has notified Medical Devices Rules, 2017 vide G.S.R. 78 (F) dated 31.01.2017 which is already implemented from 01.01.2018
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