Skip to content

SK PODO 0.276 in (7 mm) pointed orange - medium A611000731500061

by LUKAS-ERZETT GmbH & Co. KG

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 Number14027497276605 UDI-DI Date10 Feb 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  • Withdrawn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
SK PODO 0.276 in (7 mm) pointed orange - medium
Generic Name
Podiatric bur, single-use
Model / Ref / Catalog
A611000731500061
Primary DI / UDI-DI
14027497276605
FDA Product Code
GFF
GMDN Term
Podiatric bur, single-use
Device Class
Class I
Regulation Number
878.4820
GUDID distribution status
In Commercial Distribution

Other devices from LUKAS-ERZETT GmbH & Co. KG

See all devices from LUKAS-ERZETT GmbH & Co. KG →

Properties

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

Other properties (9)

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