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Surface Disinfection Verification Label Pad - Removable, Low-Tack & Latex-Free

FDA UDI

Class I (US FDA UDI)

by Cygnus Medical L.l.c.

Identity

Trade Name
Surface Disinfection Verification Label Pad - Removable, Low-Tack & Latex-Free FDA UDI
Generic Name
Device operating status label/tag, single-use FDA UDI
Device Name
Surface Disinfection Verification Label Pad - Removable, Low-Tack & Latex-Free (500 Labels per Pack, 2 Packs per Case) FDA UDI
Model / Reference
CLN33 FDA UDI
Description
Surface Disinfection Verification Label Pad - Removable, Low-Tack & Latex-Free (500 Labels per Pack, 2 Packs per Case) FDA UDI

Identifiers

Primary DI / UDI-DI
00843356101768 FDA UDI
FDA Product Code
PXV FDA UDI
GMDN Term
Device operating status label/tag, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Device operating status label/tag, single-use

Surface Disinfection Verification Label Pad - Removable, Low-Tack & Latex-Free by Cygnus Medical L.l.c. — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Device operating status label/tag, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3a1c0d98-f082-4abd-996a-14896e6cb428 33 fields · synced Jun 1, 2026