Thompson 41903ACL
by Thompson Surgical Instruments, Inc.
Thompson 41903ACL is a Class I device made by Thompson Surgical Instruments, Inc., listed in FDA GUDID since 14 Jul 2022 (UDI-DI 00841536107654), registry data as of 22 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 | Number00841536107654 | Date14 Jul 2022 | StatusListed |
Official records
- AccessGUDID record 00841536107654
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Thompson
- Generic name
- Surgical retraction system, reusable
- Model / reference
- 41903ACL
- Primary DI / UDI-DI
- 00841536107654
- FDA product code
- GAD
- GMDN term
- Surgical retraction system, reusable
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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