← Back to catalogue

Tps

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
TPS FDA UDI
Generic Name
Surgical irrigation/aspiration tubing set FDA UDI
Device Name
Reusable Irrigation Cassette FDA UDI
Model / Reference
5100050011 FDA UDI
Description
Reusable Irrigation Cassette FDA UDI

Identifiers

Catalog Number
5100-050-011 FDA UDI
Primary DI / UDI-DI
07613327174892 FDA UDI
FDA Product Code
EIA FDA UDI
GMDN Term
Surgical irrigation/aspiration tubing set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6640 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical irrigation/aspiration tubing set

Tps by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation/aspiration tubing set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 6770e283-b812-4972-a523-30b58f2581c8 35 fields · synced May 31, 2026