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Meicen

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref R-PM002

by Guangdong Meicen Medical Equipment Co., Ltd.

Identity

Trade Name
Vacuum Pump 220V EUDAMED
Meicen FDA UDI
Generic Name
Central vacuum pump FDA UDI
Device Name
Vacuum Cushions EUDAMED
Model / Reference
R-PM002 EUDAMED
/ FDA UDI

Identifiers

Primary DI / UDI-DI
06977071938102 EUDAMEDFDA UDI
Basic UDI-DI
697707193800NH EUDAMED
FDA Product Code
IOQ FDA UDI
EMDN Code
Z119099 VARIOUS BIOIMAGING AND RADIOTHERAPY INSTRUMENTS - OTHER EUDAMED
GMDN Term
Central vacuum pump FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
890.5170 FDA UDI
Market of Registration
Austria 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Central vacuum pump

Meicen by Guangdong Meicen Medical Equipment Co., Ltd. — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

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 81affd01-a9ba-4ead-9898-709045be8e7b 32 fields · synced Oct 8, 2026
  • EUDAMED 28440201-3aee-4cb7-802d-47c686485fed 61 fields · synced Jun 19, 2026