Kerlix 7884
Ref 7884Model KERLIX Super Sponges
Active
CE MDR
Valid until
Not listed
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number063014000000000000000996Z 20192253047582 | Date10 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number20192253047582 | Date23 Sep 2025 | StatusListed |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Kerlix
- Generic Name
- Woven gauze pad, non-antimicrobial
- Model / Ref / Catalog
- 7884, KERLIX Super Sponges
- Primary DI / UDI-DI
- 20192253047582
- Basic UDI-DI
- 063014000000000000000996Z
- Unit of Use DI
- 10192253047585
- FDA Product Code
- NAB
- EMDN Code
- M0201020101 Cotton gauzes, folded, without x-ray detectable thread, sterile
- GMDN Term
- Woven gauze pad, non-antimicrobial
- Device Class
- Class I
- Regulation Number
- 878.4014
- EU market of registration
- Ireland
- GUDID distribution status
- In Commercial Distribution
- Size
- Width — 15 CentimeterLength — 17 Centimeter
Other devices from Cardinal Health 200, LLC
Properties
Other properties (18)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Prescription Use: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Manufacturing Date: No