← Back to catalogue

Probe Rinse Solution

EUDAMED

Class A (EU MDR)

Ref 0320201207Model 30 mL, 50 mL, 5 mL*5Ref 0320201203

by Shenzhen Lifotronic Technology Co., Ltd.

Identity

Trade Name
Probe Rinse Solution EUDAMED
Device Name
Probe Rinse Solution EUDAMED
Model / Reference
30 mL, 50 mL, 5 mL*5 EUDAMED
0320201207 EUDAMED
0320201203 EUDAMED

Identifiers

Primary DI / UDI-DI
06978139070703 EUDAMED
06978139070710 EUDAMED
Basic UDI-DI
69703416803202025HN EUDAMED
EMDN Code
W0103010299 OTHER HAEMOGLOBIN (TYPES) TESTING - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Probe Rinse Solution by Shenzhen Lifotronic Technology Co., Ltd. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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

Manufacturer

EUDAMED SRN
CN-MF-000005654
Authorised Representative
Umedwings Netherlands B.V. NL-AR-000000444

Sources (2)

  • EUDAMED 40b62899-3e21-42a8-96c0-e3458c74c418 61 fields · synced Jul 12, 2026
  • EUDAMED 76370d4c-7ecc-4710-893d-de37b74aa2f6 61 fields · synced May 17, 2026