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TPS Small-Joint

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
TPS Small-Joint FDA UDI
Generic Name
Arthroscopic shaver system, electrically-powered FDA UDI
Device Name
[Full Radius Cutter, Arthroscopic Shaver Blade, Arthroscopic Shaver Blade, Do Not Resterilize, Do Not Use if Package is Damaged, Keep Dry, Keep Away from Sunlight] FDA UDI
Model / Reference
0275627000 FDA UDI
Description
[Full Radius Cutter, Arthroscopic Shaver Blade, Arthroscopic Shaver Blade, Do Not Resterilize, Do Not Use if Package is Damaged, Keep Dry, Keep Away from Sunlight] FDA UDI

Identifiers

Catalog Number
0275-627-000 FDA UDI
Primary DI / UDI-DI
07613327061598 FDA UDI
FDA Product Code
GFA FDA UDI
GMDN Term
Arthroscopic shaver system, electrically-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 2.5 Millimeter FDA UDI
Length — 80.0 Millimeter FDA UDI

Category: Arthroscopic shaver system, electrically-powered

TPS Small-Joint by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Arthroscopic shaver system, electrically-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 9bddede3-7187-49b3-bf4b-e0c6e3af7631 36 fields · synced Jun 8, 2026