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Thera-Cream

FDA UDI

Class II (US FDA UDI)

by Prizm Medical, Inc.

Identity

Trade Name
Thera-Cream FDA UDI
Generic Name
Electrode conductive medium FDA UDI
Model / Reference
TCT004 FDA UDI

Identifiers

Primary DI / UDI-DI
B872TCT0041 FDA UDI
510(k) Number
K032239 FDA UDI
FDA Product Code
GYB FDA UDI
GMDN Term
Electrode conductive medium FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1275 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

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

Category: Electrode conductive medium

Thera-Cream by Prizm Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrode conductive medium.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Prizm Medical, Inc.

Sources (1)

  • FDA UDI 70d1fc78-d491-4f56-ad30-2a0c1d9541a0 33 fields · synced Jun 8, 2026