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Stryker 0306-111-000

by Provision

Stryker 0306-111-000 is a Class I device made by Provision, listed in FDA GUDID since 8 Aug 2024 (UDI-DI B504TC03061110000), 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 NumberB504TC03061110000 UDI-DI Date8 Aug 2024ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Stryker
Generic name
Bone access cannula
Model / reference
0306-111-000
Primary DI / UDI-DI
B504TC03061110000
FDA product code
NBH
GMDN term
Bone access cannula
Device class
Class I
Regulation number
888.1100
GUDID distribution status
In Commercial Distribution

Related devices

Category: Bone access cannula

Similar devices

Other devices filed under FDA product code NBH (Accessories, Arthroscopic).

Other devices from Provision

See all devices from Provision →

Properties

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