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ri-medic Bluetooth®, mobile version, adult cuff an adult cuff obese, latex free
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- ri-medic Bluetooth®, mobile version, adult cuff an adult cuff obese, latex free FDA UDI
- Generic Name
- Automatic-inflation electronic sphygmomanometer, non-portable FDA UDI
- Device Name
- The ri-medic NIBP device is designed for the measurement and display of systolic and diastolic blood pressure and pulse rate. FDA UDI
- Model / Reference
- 1783 FDA UDI
- Description
- The ri-medic NIBP device is designed for the measurement and display of systolic and diastolic blood pressure and pulse rate. FDA UDI
Identifiers
- Catalog Number
- 1783 FDA UDI
- Primary DI / UDI-DI
- 04045396201262 FDA UDI
- 510(k) Number
- K070750 FDA UDI
- FDA Product Code
- DXN FDA UDI
- GMDN Term
- Automatic-inflation electronic sphygmomanometer, non-portable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1130 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
No
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
ri-medic Bluetooth®, mobile version, adult cuff an adult cuff obese, latex free by Rudolf Riester GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID
Similar devices
Also classified as Automatic-inflation electronic sphygmomanometer, non-portable.
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- microlife — MICROLIFE USA, INC. · Class II
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- AdviewII™ — American Diagnostic Corporation · Class II
Cleared under the same submission
K070750 also covers:
- Adview — American Diagnostic Corporation
- Diagnostix™ — American Diagnostic Corporation
- Diagnostix™ — American Diagnostic Corporation
- Diagnostix™ — American Diagnostic Corporation
- Diagnostix™ — American Diagnostic Corporation
- Diagnostix™ — American Diagnostic Corporation
- Diagnostix™ — American Diagnostic Corporation
- ri-medic Bluetooth®, tabletop, adult cuff and adult cuff obese, latex free — Rudolf Riester GmbH & Co. KG
- ri-medic, Bluetooth®, wall mount, adult cuff and adult cuff obese, latex free — Rudolf Riester GmbH & Co. KG
- ri-medic, mobile version, adult cuff and adult cuff obese, latex free — Rudolf Riester GmbH & Co. KG
- ri-medic, tabletop, adult cuff and adult cuff obese, latex free — Rudolf Riester GmbH & Co. KG
- ri-medic, wall mount, adult cuff and adult cuff obese, latex free — Rudolf Riester GmbH & Co. KG
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 II | Pending data |
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Manufacturer
- Manufacturer
- Rudolf Riester GmbH & Co. KG
Sources (1)
- FDA UDI 614670d8-c027-4924-9390-9f080a1df013 35 fields · synced May 31, 2026