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Cygnus

FDA UDI

Class I (US FDA UDI)

by Cygnus Medical L.l.c.

Identity

Trade Name
CYGNUS FDA UDI
Generic Name
Device operating status label/tag, single-use FDA UDI
Device Name
CLEAN CHEMO DUAL LAYER LABEL 500 PER CASE FDA UDI
Model / Reference
CCL500 FDA UDI
Description
CLEAN CHEMO DUAL LAYER LABEL 500 PER CASE FDA UDI

Identifiers

Primary DI / UDI-DI
00843356102857 FDA UDI
FDA Product Code
LYV 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

Cygnus by Cygnus Medical L.l.c. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

Manufacturer
Cygnus Medical L.l.c.

Sources (1)

  • FDA UDI 42c263e1-bd5f-4fd4-befc-1835d3a8eff9 33 fields · synced Jun 6, 2026