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Medline DYND70880

by Medline Industries, Inc.

Medline DYND70880 is a Class I device made by Medline Industries, Inc., listed in FDA GUDID since 11 Oct 2023 (UDI-DI 40884389716084), 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 Number40884389716084 UDI-DI Date11 Oct 2023ListedStatusListed 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  • Withdrawn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
Surgical hair clippers
Model / Ref / Catalog
DYND70880
Primary DI / UDI-DI
40884389716084
FDA product code
LWK
GMDN term
Surgical hair clippers
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical hair clippers

Similar devices

Other devices filed under FDA product code LWK (RAZOR, SURGICAL).

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)