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Avaline Medical NJ LLC VK97223

by Avaline Medical NJ Limited Liability Company

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810124536831 UDI-DI Date5 Dec 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Avaline Medical NJ LLC
Generic Name
Non-woven gauze pad
Model / Ref / Catalog
VK97223
Primary DI / UDI-DI
00810124536831
FDA Product Code
NAB
GMDN Term
Non-woven gauze pad
Device Class
Class I
Regulation Number
878.4014
GUDID distribution status
In Commercial Distribution

Other devices from Avaline Medical NJ Limited Liability Company

See all devices from Avaline Medical NJ Limited Liability Company →

Properties

  • Sterile
  • Single Use
  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No