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VarioVac B AGA

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref MP00504Model 208019XK19L020

by Drägerwerk AG & Co. KGaA

Identity

Trade Name
VarioVac B AGA EUDAMEDFDA UDI
Generic Name
General-purpose suction system, pneumatic FDA UDI
Model / Reference
MP00504 EUDAMEDFDA UDI
208019XK19L020 EUDAMED

Identifiers

Primary DI / UDI-DI
04048675029434 EUDAMEDFDA UDI
Basic UDI-DI
040486751208019XK19L020DY EUDAMED
Direct Marketing DI
04048675029434 EUDAMED
FDA Product Code
GCX FDA UDI
EMDN Code
A060399 FLUID COLLECTION BAGS AND SYSTEMS - OTHER EUDAMED
GMDN Term
General-purpose suction system, pneumatic FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Drägerwerk AG & Co. KGaA

Sources (2)

  • FDA UDI b267ea16-e26d-497a-bae4-9b2c54ace739 33 fields · synced Oct 7, 2026
  • EUDAMED d1ac203c-2452-41f4-a841-a89e68538f44 61 fields · synced Jul 11, 2026