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3M™ Precise™ SR-1

by 3M Company

3M™ Precise™ SR-1 is a Class I device made by 3M Company, listed in FDA GUDID since 24 Sep 2018 (UDI-DI 30707387030200), 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 Number30707387030200 UDI-DI Date24 Sep 2018ListedStatusListed 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  • Withdrawn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™ Precise™
Generic name
Skin staple remover, single-use
Model / Ref / Catalog
SR-1
Primary DI / UDI-DI
30707387030200
FDA product code
GDT
GMDN term
Skin staple remover, single-use
Device class
Class I
Regulation number
878.4760
GUDID distribution status
In Commercial Distribution

Related devices

Category: Skin staple remover, single-use

Other devices from 3M Company

See all devices from 3M Company →

Properties

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