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ThermaClear

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
ThermaClear FDA UDI
Generic Name
Surgical irrigation tubing set, single-use FDA UDI
Model / Reference
P01790 FDA UDI

Identifiers

Catalog Number
P01790 FDA UDI
Primary DI / UDI-DI
07613327626469 FDA UDI
FDA Product Code
NVT FDA UDI
GMDN Term
Surgical irrigation tubing set, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.1700 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

Category: Surgical irrigation tubing set, single-use

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

Similar devices

Also classified as Surgical irrigation tubing set, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 3e4baf07-7145-4f8b-8ed4-df9f390627fe 34 fields · synced May 30, 2026