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VarioVac B BS

FDA UDIEUDAMED

Class II (US FDA UDI)

by Drägerwerk AG & Co. KGaA

Identity

Trade Name
VarioVac B BS FDA UDI
Generic Name
General-purpose suction system, pneumatic FDA UDI
Model / Reference
MP00502 FDA UDI

Identifiers

Primary DI / UDI-DI
04048675029410 FDA UDI
FDA Product Code
GCX FDA UDI
GMDN Term
General-purpose suction system, pneumatic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: General-purpose suction system, pneumatic

VarioVac B BS by Drägerwerk AG & Co. KGaA — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose suction system, pneumatic.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI e33110eb-2a99-4345-ac43-e52dfc5b48ea 33 fields · synced Jun 19, 2026
  • EUDAMED 1 fields · synced Jun 19, 2026