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Sheath
EUDAMEDClass A (EU MDR)
Ref Sheath-sys 20LModel Sheath-Sys,Sheath-Ruby,Sheath-XN
Identity
- Device Name
- Sheath EUDAMED
- Model / Reference
- Sheath-Sys,Sheath-Ruby,Sheath-XN EUDAMEDSheath-sys 20L EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06972337857821 EUDAMED
- Basic UDI-DI
- 697233785Sheath022NM EUDAMED
- EMDN Code
- W0103010105 CBC-REAGENTS (CLEANING-/DILUTING-/LYSING-/SHEATH-FLUIDS) EUDAMED
Classification
- Device Class
- Class A EUDAMED
- Market of Registration
- Austria 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
Sheath by B&E Bio-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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDR | 697233785Sheath022NM | Class A | Active |
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Manufacturer
- Manufacturer
- B&E Bio-Technology Co., Ltd.
- EUDAMED SRN
- CN-MF-000023256
- Authorised Representative
- SUNGO Europe B.V. NL-AR-000000247
Sources (1)
- EUDAMED 1165b7b9-f4b8-4620-a73d-89b246e42059 61 fields · synced Jun 18, 2026