← Back to catalogue

312/DS/3.32/2 57cm wide lift-off top shield

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 312/DS/3.32/2

by Kenex (Electro-Medical) Limited

Identity

Trade Name
312/DS/3.32/2 57cm wide lift-off top shield EUDAMED
KENEX FDA UDI
Generic Name
Radiation shielding curtain FDA UDI
Device Name
Table mounted radiation shields EUDAMED
312/DS/3.32/2 57cm wide lift-off top shield FDA UDI
Model / Reference
312/DS/3.32/2 EUDAMEDFDA UDI
Description
312/DS/3.32/2 57cm wide lift-off top shield FDA UDI

Identifiers

Catalog Number
312/DS/3.32/2 FDA UDI
Primary DI / UDI-DI
05055449406154 EUDAMEDFDA UDI
Basic UDI-DI
50554494SHTXZ EUDAMED
Direct Marketing DI
05055449406154 EUDAMED
FDA Product Code
KPY FDA UDI
EMDN Code
Z11030503 PATIENT TABLES FOR RADIOLOGICAL EQUIPMENT EUDAMED
GMDN Term
Radiation shielding curtain FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
892.6500 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

312/DS/3.32/2 57cm wide lift-off top shield by Kenex (electro-Medical) Limited — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

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
GB-MF-000009022
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED c4fdcc17-8c71-47d7-b5e0-7a2ae0eee1f7 61 fields · synced Jun 18, 2026
  • FDA UDI 34837654-20e0-4da6-80a9-e918e1dd8c39 34 fields · synced May 30, 2026