Stephens Instruments S7-1315
Ref S7-1315
Stephens Instruments S7-1315 is a Class I device made by Krishna Imports Inc, registered in EUDAMED on 2 Jun 2026 (Basic UDI-DI B-00810799036872) and listed in FDA GUDID since 22 Sep 2020 (UDI-DI 00810799036872), active as of 22 Oct 2026.
Active
CE MDD
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-00810799036872 00810799036872 | Date2 Jun 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00810799036872 | Date22 Sep 2020 | StatusListed |
Official records
- EUDAMED public site B-00810799036872
- AccessGUDID record 00810799036872
Across registries
- EUDAMED Basic UDI-DI B-00810799036872 registered 2 Jun 2026 Active
- FDA GUDID UDI-DI 00810799036872 listed 22 Sep 2020 Listed
Timeline
- Listed FDA GUDID 00810799036872
- Registered EUDAMED B-00810799036872
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Stephens Instruments
- Generic name
- Conjunctival scissors, reusable
- Model / Ref / Catalog
- S7-1315
- Primary DI / UDI-DI
- 00810799036872
- Basic UDI-DI
- B-00810799036872
- FDA product code
- HNF
- EMDN code
- L01040501 Corneal scissors, reusable
- GMDN term
- Conjunctival scissors, reusable
- Device class
- Class I
- Regulation number
- 886.4350
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Norway
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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