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Medline 27710321RH

by Medline Industries, Inc.

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 Number10888277405202 UDI-DI Date8 Apr 2022ListedStatusListed 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  • Withdrawn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
Medline
Generic name
Orthopaedic bur, single-use
Model / Ref / Catalog
27710321RH
Primary DI / UDI-DI
10888277405202
FDA product code
GFF
GMDN term
Orthopaedic bur, single-use
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution

Related devices

Category: Orthopaedic bur, single-use

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number

Other properties (10)

  • Sterilise before use: No
  • Implantable: No
  • Contains latex: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Serial number: No
  • Expiration date: No
  • Manufacturing date: No