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3M™ Steri-Strip™ E4542

by 3M Company 2 variants

3M™ Steri-Strip™ E4542 is a Class I device made by 3M Company, listed in FDA GUDID since 8 Mar 2021 (UDI-DI 00707387804558), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00707387804558 UDI-DI Date8 Mar 2021ListedStatusListed 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  • Withdrawn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
3M™ Steri-Strip™
Generic name
Skin-closure adhesive strip
Model / Ref / Catalog
E4542
Primary DI / UDI-DI
00707387804558
FDA product code
KGX
GMDN term
Skin-closure adhesive strip
Device class
Class I
Regulation number
880.5240
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KGX (Tape and bandage, adhesive).

Other devices from 3M Company

See all devices from 3M Company →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)