Merocel™ 400416
Merocel 400416 is a dissection sponge (FDA unclassified) made by Medtronic Xomed Inc, listed in FDA GUDID since 4 Mar 2022 (UDI-DI 20763000616834), registry data as of 8 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number20763000616834 | Date4 Mar 2022 | StatusListed |
Official records
- AccessGUDID record 20763000616834
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Merocel™
- Generic name
- Dissection sponge
- Model / reference
- 400416
- Primary DI / UDI-DI
- 20763000616834
- FDA product code
- EFQ, NAB
- GMDN term
- Dissection sponge
- Device class
- U
- Regulation number
- 878.4014
- GUDID distribution status
- In Commercial Distribution
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Other devices filed under FDA product code EFQ (GAUZE/SPONGE, INTERNAL).
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- SPONGE, SURGICAL, GAUZE, COMPRESSED 2 BY 2 INCHES by Fraass Survival Systems, Inc.
- 18X36, 36X36, 18X72, 24X72 GAUZE COMPRESS by Advantage Credit Services, Inc.