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StrykeCam P45000

by STRYKER Communications, Inc.

StrykeCam P45000 is a Class I device made by STRYKER Communications, Inc., listed in FDA GUDID since 28 Feb 2020 (UDI-DI 07613327502046), 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 Number07613327502046 UDI-DI Date28 Feb 2020ListedStatusListed 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  • Withdrawn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
StrykeCam
Generic name
Surgical video camera
Model / Ref / Catalog
P45000
Primary DI / UDI-DI
07613327502046
FDA product code
KQM
GMDN term
Surgical video camera
Device class
Class I
Regulation number
878.4160
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical video camera

Similar devices in this category

Other devices filed under Surgical video camera.

Other devices from STRYKER Communications, Inc.

See all devices from STRYKER Communications, Inc. →

Properties

  • Premarket exempt
  • Serial number
Other properties (13, all answered No)