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TempProbe™

FDA UDI

Class II (US FDA UDI)

by Endocare, Inc.

Identity

Trade Name
TempProbe™ FDA UDI
Generic Name
Cryosurgical set FDA UDI
Device Name
Endocare™ TempProbe™ Device FDA UDI
Model / Reference
CRYO-55-F FDA UDI
Description
Endocare™ TempProbe™ Device FDA UDI

Identifiers

Catalog Number
CRYO-55-F FDA UDI
Primary DI / UDI-DI
00810563020120 FDA UDI
510(k) Number
K153489 FDA UDI
FDA Product Code
GEH FDA UDI
GMDN Term
Cryosurgical set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4350 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cryosurgical set

TempProbe™ by Endocare, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cryosurgical set.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Endocare, Inc.

Sources (1)

  • FDA UDI b3b700fc-75b9-4b31-94e3-c258dcbf8704 36 fields · synced May 30, 2026