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Protekt Blood Pressure Monitor, Digital, Auto Inflate w/ Batteries
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Protekt Blood Pressure Monitor, Digital, Auto Inflate w/ Batteries FDA UDI
- Generic Name
- Automatic-inflation electronic sphygmomanometer, portable, arm/wrist FDA UDI
- Device Name
- Protekt Blood Pressure Monitor, Digital, Auto Inflate w/ Batteries FDA UDI
- Model / Reference
- PMDBPA FDA UDI
- Description
- Protekt Blood Pressure Monitor, Digital, Auto Inflate w/ Batteries FDA UDI
Identifiers
- Catalog Number
- PMDBPA FDA UDI
- Primary DI / UDI-DI
- 05060488570933 FDA UDI
- 510(k) Number
- K150545 FDA UDI
- FDA Product Code
- DXN FDA UDI
- GMDN Term
- Automatic-inflation electronic sphygmomanometer, portable, arm/wrist 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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Height — 6 Inch FDA UDIWidth — 12 Inch FDA UDILength — 6 Inch FDA UDI
Category: Automatic-inflation electronic sphygmomanometer, portable, arm/wrist
Protekt Blood Pressure Monitor, Digital, Auto Inflate w/ Batteries by Proactive Medical Products — Class II — FDA UDI — listed in FDA GUDID
Similar devices
Also classified as Automatic-inflation electronic sphygmomanometer, portable, arm/wrist.
- Arm Type Automatic Blood Pressure Monitor — Shenzhen Jiacom Technology Co., Ltd · Class II
- Dario Smart Monitor (Cellular) - Blood Pressure Monitoring System — DARIOHEALTH CORP. · Class II
- MoDash — Shenzhen Urion Technology Co., Ltd. · Class II
- Veridian Healthcare — VERIDIAN HEALTHCARE · Class II
- Welch Allyn, Inc. — Welch Allyn, Inc. · Class II
- BRIGHT LIFE — Shenzhen Urion Technology Co., Ltd. · Class II
- RemoteCare 4U — Guangdong Transtek Medical Electronics Co., Ltd · Class II
- Omron 3 Series Upper Arm Blood Pressure Monitor — Omron Healthcare, Inc. · Class II
Cleared under the same submission
K150545 also covers:
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Proactive Medical Products
Sources (1)
- FDA UDI 96e2ea9b-8c5d-4eae-be94-c1a4ce4a7480 37 fields · synced May 30, 2026