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nexoderm® Biopsy Punch Ø 3, 0 mm 20021

by sfm medical devices GmbH

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04063574200210 UDI-DI Date28 Sep 2026ListedStatusListed 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  • Withdrawn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
nexoderm® Biopsy Punch Ø 3,0 mm
Generic Name
Skin-coring punch, single-use
Model / Reference
20021
Primary DI / UDI-DI
04063574200210
FDA Product Code
LRY
GMDN Term
Skin-coring punch, single-use
Device Class
Class I
Regulation Number
878.4800
GUDID distribution status
In Commercial Distribution

Other devices from sfm medical devices GmbH

See all devices from sfm medical devices GmbH →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No