← Back to catalogue

Vacumaspirator Diss Canada

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref MP00687Model 208019XK19L020

by Drägerwerk AG & Co. KGaA

Identity

Trade Name
Vakuumabsaugung Diss Kanada EUDAMED
Vacumaspirator Diss Canada FDA UDI
Generic Name
Vacuum suction regulator/regulation set, general-purpose FDA UDI
Model / Reference
MP00687 EUDAMEDFDA UDI
208019XK19L020 EUDAMED

Identifiers

Primary DI / UDI-DI
04048675389569 EUDAMEDFDA UDI
Basic UDI-DI
040486751208019XK19L020DY EUDAMED
Direct Marketing DI
04048675389569 EUDAMED
FDA Product Code
GCX FDA UDI
EMDN Code
A060399 FLUID COLLECTION BAGS AND SYSTEMS - OTHER EUDAMED
GMDN Term
Vacuum suction regulator/regulation set, general-purpose 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Vacuum suction regulator/regulation set, general-purpose

Vacumaspirator Diss Canada by Drägerwerk AG & Co. KGaA — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Vacuum suction regulator/regulation set, general-purpose.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (2)

  • FDA UDI 8f1defe2-d6c2-4526-82d7-89250c59a613 33 fields · synced Jul 17, 2026
  • EUDAMED 49cefaea-b00c-4a6c-b163-8fef97b8733f 61 fields · synced Jul 17, 2026