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Ans Medical

FDA UDI

Class I (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
ANS MEDICAL FDA UDI
Generic Name
Patient medical adhesive remover FDA UDI
Device Name
TENS Clean Cote, Nonsterile, FDA UDI
Model / Reference
UP220 FDA UDI
Description
TENS Clean Cote, Nonsterile, FDA UDI

Identifiers

Catalog Number
MS71175 FDA UDI
Primary DI / UDI-DI
10884521738362 FDA UDI
FDA Product Code
KOX FDA UDI
GMDN Term
Patient medical adhesive remover FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4730 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Patient medical adhesive remover

Ans Medical by Cardinalhealth — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient medical adhesive remover.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 0c12b9bf-6f20-4671-ac47-d9eed4650fdb 34 fields · synced May 29, 2026