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Rps 8800512000

by Stryker Corp.

Rps 8800512000 (8800-512-000) is an instrument tray (FDA Class I; FDA product code FSM, Tray, Surgical, Instrument) made by Stryker Corp., listed in FDA GUDID since 1 Oct 2025 (UDI-DI 07613327631876), 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 Number07613327631876 UDI-DI Date1 Oct 2025ListedStatusListed 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  • Withdrawn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
Rps
Generic name
Instrument tray, reusable
Model / Ref / Catalog
8800512000, 8800-512-000
Primary DI / UDI-DI
07613327631876
FDA product code
FSM
GMDN term
Instrument tray, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code FSM (TRAY, SURGICAL, INSTRUMENT).

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)