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Single Use Specimen Bag

EUDAMED

Class IIa (EU MDR)

Ref LTX-TRB-A1500Model LTX-TRB-A150

by Suzhou Lantex Medical Technology Company Limited

Identity

Device Name
Single Use Specimen Bag EUDAMED
Model / Reference
LTX-TRB-A150 EUDAMED
LTX-TRB-A1500 EUDAMED

Identifiers

Primary DI / UDI-DI
06971062273098 EUDAMED
Basic UDI-DI
697106227TRBAL5 EUDAMED
EMDN Code
G03050199 DIGESTIVE ENDOSCOPY, RETRIEVAL DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

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

Single Use Specimen Bag by Suzhou Lantex Medical Technology Company Limited — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000039444
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 4eddd277-3c9f-4e35-84a4-3633a547c588 61 fields · synced Jun 19, 2026