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Rps 8825185075

by Stryker Corp.

Rps 8825185075 (8825-185-075) is a surgical saw blade (FDA Class II; FDA product code OLO, Orthopedic stereotaxic instrument) made by Stryker Corp., listed in FDA GUDID since 7 Oct 2025 (UDI-DI 07613327645002), 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 Number07613327645002 UDI-DI Date7 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  • Withdrawn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
Surgical saw blade, oscillating, single-use
Model / Ref / Catalog
8825185075, 8825-185-075
Primary DI / UDI-DI
07613327645002
FDA product code
OLO
GMDN term
Surgical saw blade, oscillating, single-use
Device class
Class II
Regulation number
882.4560
GUDID distribution status
In Commercial Distribution
Size
Depth — 75.0 Millimeter

Similar devices

Other devices filed under FDA product code OLO (Orthopedic stereotaxic instrument).

Other devices from Stryker Corp.

See all devices from Stryker Corp. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)