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0306610000

by Stryker Corp.

0306610000 is a Class I device made by Stryker Corp., listed in FDA GUDID since 24 Sep 2018 (UDI-DI 04546540899439), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04546540899439 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  • Withdrawn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

Generic name
Orthopaedic implantable material dispenser, cartridge-/syringe-accepting, reusable
Model / Ref / Catalog
0306610000
Primary DI / UDI-DI
04546540899439
FDA product code
JDZ
GMDN term
Orthopaedic implantable material dispenser, cartridge-/syringe-accepting, reusable
Device class
Class I
Regulation number
888.4210
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic cement/bone filler dispensing gun

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Other devices filed under Orthopaedic cement/bone filler dispensing gun.

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
Other properties (12, all answered No)