Identity
- Trade Name
- IntelliVue CL NBP Pod FDA UDI
- Generic Name
- Automatic-inflation electronic sphygmomanometer, portable, arm/wrist FDA UDI
- Device Name
- IntelliVue Cableless NBP Pod, a battery-powered non-invasive blood pressure device for Cableless Monitoring of patients. The IntelliVue CL NBP Pod provides non-invasive blood pressure and pulse rate via short range radio to the receiving system. FDA UDI
- Model / Reference
- IntelliVue CL NBP Pod FDA UDI
- Description
- IntelliVue Cableless NBP Pod, a battery-powered non-invasive blood pressure device for Cableless Monitoring of patients. The IntelliVue CL NBP Pod provides non-invasive blood pressure and pulse rate via short range radio to the receiving system. FDA UDI
Identifiers
- Catalog Number
- 865216 FDA UDI
- Primary DI / UDI-DI
- 00884838020672 FDA UDI
- FDA Product Code
- DRG FDA UDI
- GMDN Term
- Automatic-inflation electronic sphygmomanometer, portable, arm/wrist FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2910 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
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
MR Unsafe FDA UDI
Category: Automatic-inflation electronic sphygmomanometer, portable, arm/wrist
IntelliVue CL NBP Pod by Philips Medizin Systeme Böblingen GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Automatic-inflation electronic sphygmomanometer, portable, arm/wrist.
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- RemoteCare 4U — Guangdong Transtek Medical Electronics Co., Ltd · Class II
- Omron 3 Series Upper Arm Blood Pressure Monitor — Omron Healthcare, Inc. · 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 II | Pending data |
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Manufacturer
- Manufacturer
- Philips Medizin Systeme Böblingen GmbH
Sources (1)
- FDA UDI 5a92b090-2e1c-44e6-a972-5187570a482d 36 fields · synced Jun 8, 2026