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0502880201

by Stryker Corp.

0502880201 (0502-880-201) is a Class II device made by Stryker Corp., listed in FDA GUDID since 23 Sep 2016 (UDI-DI 07613327060331), 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 Number07613327060331 UDI-DI Date23 Sep 2016ListedStatusListed 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  • Withdrawn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

Generic name
Urethral dilator, reusable
Model / Ref / Catalog
0502880201, 0502-880-201
Primary DI / UDI-DI
07613327060331
FDA product code
HIH, KQT, FAS, FAJ
GMDN term
Urethral dilator, reusable
Device class
Class II
Regulation number
884.1690, 876.4370, 876.4300, 876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Urethral dilator, reusableUrethrotome

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)