← Back to catalogue
NIBP Cuffs
EUDAMEDFDA UDIClass I (EU MDR)
Ref 2.120020Model BPCV14XS - Velcro cuff XS
by Schiller Ag
Identity
- Trade Name
- NIBP Cuffs EUDAMEDNIBP MCF CV 18-26 BA PED EUDAMEDSchiller NIBP cuff FDA UDI
- Generic Name
- Blood pressure cuff, reusable FDA UDI
- Device Name
- BPCV14XS EUDAMEDNIBP MCF CV 18-26 BA PED FDA UDI
- Model / Reference
- BPCV14XS - Velcro cuff XS EUDAMED2.120020 EUDAMEDFDA UDI
- Description
- NIBP MCF CV 18-26 BA PED FDA UDI
Identifiers
- Catalog Number
- 2.120020 FDA UDI
- Primary DI / UDI-DI
- 07613365000528 EUDAMEDFDA UDI
- Basic UDI-DI
- 761336500000000452 EUDAMED
- Direct Marketing DI
- 07613365000528 EUDAMED
- FDA Product Code
- DXQ FDA UDI
- EMDN Code
- Z1203020302 NON–INVASIVE BLOOD PRESSURE MONITORING INSTRUMENTS EUDAMED
- GMDN Term
- Blood pressure cuff, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 870.1120 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
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
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
NIBP Cuffs by Schiller AG — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 761336500000000452 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Schiller Ag
- EUDAMED SRN
- CH-MF-000012722
- Authorised Representative
- SCHILLER Medizintechnik GmbH DE-AR-000006934
Sources (3)
- EUDAMED c4d33c3e-c998-4a4d-96ed-37339a771075 61 fields · synced Jul 15, 2026
- FDA UDI 8e7e4dad-cc85-4fb0-9adb-abf39b21f4a8 37 fields · synced May 30, 2026
- EUDAMED 5ce3d4ef-cf49-4e3a-8a2f-e8d09d05253b 61 fields · synced Jul 15, 2026