Kerlix 2949
Kerlix 2949 is a Class I device made by Cardinalhealth, listed in FDA GUDID since 23 Jun 2018 (UDI-DI 10884527016631), 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 | Number10884527016631 | Date23 Jun 2018 | StatusListed |
Official records
- AccessGUDID record 10884527016631
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Kerlix
- Generic name
- Radiopaque woven surgical sponge
- Model / Ref / Catalog
- 2949
- Primary DI / UDI-DI
- 10884527016631
- FDA product code
- GDY
- GMDN term
- Radiopaque woven surgical sponge
- Device class
- Class I
- Regulation number
- 878.4450
- GUDID distribution status
- In Commercial Distribution
- Size
- Outer Diameter — 1.625 Inch
Similar devices
Other devices filed under FDA product code GDY (GAUZE/SPONGE, INTERNAL, X-RAY DETECTABLE).
- GAUZE & LAB SPONGES STERILE & NON by Ulti-Med Intl., Inc.
- STRUNG NEURO SPONGE PATTIES-X-RAY- by Ormed Mfg., Inc.
- GREEN RADIOPAQUE IN SURG. SPONGES by Kendall Research Center
- SURGICAL DRESSINGS by Foreign Trade Zone of Wisconsin
- TRIANGULAR SPONGES by Medical Perspectives Corp.
- LAPAROTOMY SPONGES by American Healthcare, Inc.
- TOMAC STERILE DISP. LAP SPONGE by American Convertors Div., American Pharmaseal
- SPONGE, LAPAROTOMY, VARIOUS SIZE by Shawnee Products, Inc.
- Symmetry SECTO® 81-1000 by Aspen Surgical Products, Inc.
- Expanding ear tampon 66410 by Spiggle & Theis Medizintechnik GmbH