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Duplex

FDA UDI

Class I (US FDA UDI)

by Cygnus Medical L.l.c.

Identity

Trade Name
Duplex FDA UDI
Generic Name
Instrument hygienic-transportation bag FDA UDI
Device Name
DUAL-CAVITY instrument transport bag FDA UDI
Model / Reference
DCB2017 FDA UDI
Description
DUAL-CAVITY instrument transport bag FDA UDI

Identifiers

Primary DI / UDI-DI
00843356101065 FDA UDI
FDA Product Code
PXV FDA UDI
GMDN Term
Instrument hygienic-transportation bag 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: Instrument hygienic-transportation bag

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

Similar devices

Also classified as Instrument hygienic-transportation bag.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d85f9828-4142-424f-973f-76a19e69792d 33 fields · synced May 30, 2026