Identity
- Trade Name
- Blood Pressure Meter FDA UDI
- Generic Name
- Aneroid manual sphygmomanometer FDA UDI
- Device Name
- The Blood Pressure Meter is a manual non-invasive aneroid sphygmomanometer which respectively uses an inflation cuff wrapped around the upper arm. The cuff is inflated and deflated by a manual inflation bulb. Besides a manometer (Aneroid gauge), the accessories include additional stethoscope. It is conjunction with Stethoscope when use. FDA UDI
- Model / Reference
- Model Max0203 (Blue, Pink or Black cuff) FDA UDI
- Description
- The Blood Pressure Meter is a manual non-invasive aneroid sphygmomanometer which respectively uses an inflation cuff wrapped around the upper arm. The cuff is inflated and deflated by a manual inflation bulb. Besides a manometer (Aneroid gauge), the accessories include additional stethoscope. It is conjunction with Stethoscope when use. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06972243188279 FDA UDI
- 510(k) Number
- K190902 FDA UDI
- FDA Product Code
- DXQ FDA UDI
- GMDN Term
- Aneroid manual sphygmomanometer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1120 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
Yes
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
Yes
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: Aneroid manual sphygmomanometer
Blood Pressure Meter by Wenzhou Renhua Instruments Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Aneroid manual sphygmomanometer.
- Diagnostix™ — American Diagnostic Corporation · Class II
- Diagnostix™ — American Diagnostic Corporation · Class II
- e-mega® black, disinfectable one-piece cuff, small adult size 2-tube — Rudolf Riester GmbH & Co. KG · Class II
- Diagnostix™ — American Diagnostic Corporation · Class II
- Princess — American Diagnostic Corporation · Class II
- Diagnostix™ — American Diagnostic Corporation · Class II
- E-sphyg™ — American Diagnostic Corporation · Class II
- BAUM — W.A. BAUM CO., INC. · Class II
Cleared under the same submission
K190902 also covers:
- HOMEDICS — FKA DISTRIBUTING CO., LLC
- My Medic — My Medic
- PARAMED — SILEX GLOBAL LLC
- PARAMED — SILEX GLOBAL LLC
- PARAMED — SILEX GLOBAL LLC
- PARAMED — SILEX GLOBAL LLC
- PARAMED — SILEX GLOBAL LLC
- PARAMED — SILEX GLOBAL LLC
- Blood Pressure Meter — Wenzhou Renhua Instruments Co., Ltd.
- Blood Pressure Meter — Wenzhou Renhua Instruments Co., Ltd.
- Blood Pressure Meter — Wenzhou Renhua Instruments Co., Ltd.
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
- Wenzhou Renhua Instruments Co., Ltd.
Sources (1)
- FDA UDI 2c8cc7fe-f415-47d0-b6e1-15768af158dd 34 fields · synced May 30, 2026