Surgistar 961618
Surgistar 961618 is a Class I device made by Surgistar Inc., listed in FDA GUDID since 7 Oct 2019 (UDI-DI 00878799004000), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00878799004000 | Date7 Oct 2019 | StatusListed |
Official records
- AccessGUDID record 00878799004000
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Surgistar
- Generic name
- Scalpel, single-use
- Model / reference
- 961618
- Primary DI / UDI-DI
- 00878799004000
- FDA product code
- EMF
- GMDN term
- Scalpel, single-use
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- In Commercial Distribution
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- KIATO 13 14813 by ADITYA DISPOMED PRODUCTS PRIVATE LIMITED
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