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Medline 71070349RH

by Medline Industries, Inc.

Medline 71070349RH is a Class I device made by Medline Industries, Inc., listed in FDA GUDID since 18 May 2022 (UDI-DI 10888277337213), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10888277337213 UDI-DI Date18 May 2022ListedStatusListed GUDID: in commercial distribution

Official records

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  • Withdrawn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
Fluted surgical drill bit, single-use
Model / Ref / Catalog
71070349RH
Primary DI / UDI-DI
10888277337213
FDA product code
GFG
GMDN term
Fluted surgical drill bit, single-use
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)