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Carina VPack NIV ClasS Fullf M

FDA UDI

Class I (US FDA UDI)

by Drägerwerk AG & Co. KGaA

Identity

Trade Name
Carina VPack NIV ClasS Fullf M FDA UDI
Generic Name
Microbial medical gas filter, single-use FDA UDI
Model / Reference
MP01664 FDA UDI

Identifiers

Primary DI / UDI-DI
04048675421092 FDA UDI
FDA Product Code
CAI FDA UDI
GMDN Term
Microbial medical gas filter, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5240 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Ventilator breathing circuit, single-useMicrobial medical gas filter, single-useRebreathing oxygen face maskNon-rebreathing valve, reusable

Carina VPack NIV ClasS Fullf M by Drägerwerk AG & Co. KGaA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-rebreathing valve, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 41ca56d0-d148-4e9e-8160-fd75e48e7908 33 fields · synced May 30, 2026