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Clear Infusor 500 ml

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 57-08-050

by VBM Medizintechnik GmbH

Identity

Trade Name
Clear Infusor 500 ml EUDAMED
Clear Infusor FDA UDI
Generic Name
Intravenous pressure infusor, manual, reusable FDA UDI
Device Name
Pressure Infusion Cuffs - Clear Infusor EUDAMED
500 ml FDA UDI
Model / Reference
57-08-050 EUDAMEDFDA UDI
Description
500 ml FDA UDI

Identifiers

Primary DI / UDI-DI
14250105629429 EUDAMEDFDA UDI
Basic UDI-DI
42501056-2.6.2-WA EUDAMED
Direct Marketing DI
04250105629422 EUDAMED
FDA Product Code
KZD FDA UDI
EMDN Code
A080299 INFUSION BAGS AND CONTAINERS, SINGLE-USE - OTHER EUDAMED
GMDN Term
Intravenous pressure infusor, manual, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
880.5420 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

Yes

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

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Total Volume — 500 Milliliter FDA UDI

Category: Intravenous administration bag/bottle

Clear Infusor 500 ml by VBM Medizintechnik GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravenous administration bag/bottle.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
DE-MF-000005907

Sources (2)

  • EUDAMED 6980243f-b0a8-4d50-bac7-831e1c99ec45 61 fields · synced Jun 17, 2026
  • FDA UDI 78d9114d-9dde-49fa-84b2-b074b6dc648d 36 fields · synced May 30, 2026