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Accessory patient gas pathway expiratory only
EUDAMEDClass I (EU MDR)
Ref V-861360
Identity
- Device Name
- Accessory patient gas pathway expiratory only EUDAMED
- Model / Reference
- V-861360 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04250892908281 EUDAMED
- Basic UDI-DI
- 42508929011861QE EUDAMED
- Direct Marketing DI
- 04250892908281 EUDAMED
- EMDN Code
- Z12159085 VARIOUS PNEUMOLOGY AND RESPIRATORY PHYSIOPATHOLOGY INSTRUMENTS - CONSUMABLES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
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
Accessory patient gas pathway expiratory only by Jaeger Medical GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 42508929011861QE | Class I | Active |
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Manufacturer
- Manufacturer
- Jaeger Medical GmbH
- EUDAMED SRN
- DE-MF-000007090
Sources (1)
- EUDAMED 98a73a5f-480f-450f-baaf-ed8975f76eee 61 fields · synced Jun 19, 2026