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Centurion SR60610

by Centurion Medical Products

Centurion SR60610 is a Class I device made by Centurion Medical Products, listed in FDA GUDID since 2 Jan 2022 (UDI-DI 10653160280507), 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 Number10653160280507 UDI-DI Date2 Jan 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  • Withdrawn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
Centurion
Generic name
Suture removal kit
Model / Ref / Catalog
SR60610
Primary DI / UDI-DI
10653160280507
FDA product code
MCZ
GMDN term
Suture removal kit
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Suture removal kit

Other devices from Centurion Medical Products

See all devices from Centurion Medical Products →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (8, all answered No)