Identity
- Trade Name
- RVS-200, NIBP(Riester) +SpO2(Nellcor) + Pred. Temp FDA UDI
- Generic Name
- Automatic-inflation electronic sphygmomanometer, non-portable FDA UDI
- Device Name
- The RVS-200 Wall Diagnostic Station and RVS-200 Extension Module were produced for use with various instrument heads for non-invasive diagnosis of ENT and Ophthalmology. FDA UDI
- Model / Reference
- 1961-RNBXU FDA UDI
- Description
- The RVS-200 Wall Diagnostic Station and RVS-200 Extension Module were produced for use with various instrument heads for non-invasive diagnosis of ENT and Ophthalmology. FDA UDI
Identifiers
- Catalog Number
- 1961-RNBXU FDA UDI
- Primary DI / UDI-DI
- 04045396000339 FDA UDI
- FDA Product Code
- ERA FDA UDI
- GMDN Term
- Automatic-inflation electronic sphygmomanometer, non-portable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4770 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Automatic-inflation electronic sphygmomanometer, non-portable
RVS-200, NIBP(Riester) +SpO2(Nellcor) + Pred. Temp by Rudolf Riester GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Automatic-inflation electronic sphygmomanometer, non-portable.
- Blood Pressure Monitor CH-4532 — CITIZEN SYSTEMS JAPAN CO., LTD. · Class II
- Diagnostix™ — American Diagnostic Corporation · Class II
- Spotskan — Skanray Technologies · Class II
- PORTAL724 — Shenzhen Belter Health Measurement and Analysis Technology Co., Ltd. · Class II
- microlife — MICROLIFE USA, INC. · Class II
- A&D Medical — A & D Co., Ltd. · Class II
- Tango M2 — SUNTECH MEDICAL, INC. · Class II
- AdviewII™ — American Diagnostic Corporation · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| 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
- Rudolf Riester GmbH & Co. KG
Sources (1)
- FDA UDI 50f6d746-772e-4441-9c48-7c9a3fd3a732 34 fields · synced May 30, 2026