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Kerlix 2949

by Cardinalhealth

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 FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10884527016631 UDI-DI Date23 Jun 2018ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

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).

Other devices from Cardinalhealth

See all devices from Cardinalhealth →

Properties

  • Single use
  • Contains latex
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)