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MedK Manifold Sets
EUDAMEDClass IIa (EU MDR)
Ref 982503GRF010600Model MedK Manifold Sets
by medK GmbH
Identity
- Device Name
- MedK Manifold Sets EUDAMED
- Model / Reference
- MedK Manifold Sets EUDAMED982503GRF010600 EUDAMED
Identifiers
- Primary DI / UDI-DI
- +B827982503GRF0106001 EUDAMED
- Basic UDI-DI
- B-+B827982503GRF0106001 EUDAMED
- EMDN Code
- A0702 RAMPS EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Germany 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
MedK Manifold Sets by medK GmbH — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-+B827982503GRF0106001 | Class IIa | Active |
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Manufacturer
- Manufacturer
- medK GmbH
- EUDAMED SRN
- DE-MF-000006273
Sources (1)
- EUDAMED 06f92170-3969-416b-b6ec-569996e992a0 61 fields · synced Jul 16, 2026