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Medline 7207315RH

by Medline Industries, Inc.

Medline 7207315RH is a Class I device made by Medline Industries, Inc., listed in FDA GUDID since 3 Jan 2025 (UDI-DI 10888277384439), 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 Number10888277384439 UDI-DI Date3 Jan 2025ListedStatusListed 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  • Withdrawn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
Cannulated surgical drill bit, single-use
Model / Ref / Catalog
7207315RH
Primary DI / UDI-DI
10888277384439
FDA product code
GFG
GMDN term
Cannulated surgical drill bit, single-use
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution

Related devices

Category: Cannulated surgical drill bit, single-use

Similar devices in this category

Other devices filed under Cannulated surgical drill bit, single-use.

Other devices from Medline Industries, Inc.

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Properties

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