Identity
- Trade Name
- CPRmeter 2 (Multi-bundle) FDA UDI
- Generic Name
- Cardiopulmonary resuscitation feedback device, electronic FDA UDI
- Device Name
- The CPRmeter 2 CPR feedback device is a portable, battery-powered device intended to provide real-time feedback on manual chest compression (i.e depth of compression) performed during cardiopulmonary resuscitation (CPR) on a patient in cardiac arrest, or during training on a resuscitation training model. It typically consists of a chest plate with a digital display, which is placed on the sternum and pushed down during chest compression and will display compression depth and rate, measured by one of various electronic technologies (e.g., electromagnetic signaling to a baseplate, accelerometer). It is intended to be used by those trained in CPR. FDA UDI
- Model / Reference
- 801 FDA UDI
- Description
- The CPRmeter 2 CPR feedback device is a portable, battery-powered device intended to provide real-time feedback on manual chest compression (i.e depth of compression) performed during cardiopulmonary resuscitation (CPR) on a patient in cardiac arrest, or during training on a resuscitation training model. It typically consists of a chest plate with a digital display, which is placed on the sternum and pushed down during chest compression and will display compression depth and rate, measured by one of various electronic technologies (e.g., electromagnetic signaling to a baseplate, accelerometer). It is intended to be used by those trained in CPR. FDA UDI
Identifiers
- Catalog Number
- 801-00249 FDA UDI
- Primary DI / UDI-DI
- 07045432073355 FDA UDI
- FDA Product Code
- LIX FDA UDI
- GMDN Term
- Cardiopulmonary resuscitation feedback device, electronic FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.5210 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
Category: Cardiopulmonary resuscitation feedback device, electronic
CPRmeter 2 (Multi-bundle) by Laerdal Medical Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cardiopulmonary resuscitation feedback device, electronic.
- Beaty — MEDICAL FEEDBACK TECHNOLOGIES LTD · Class II
- TrueCPR™ Coaching Device — PHYSIO-CONTROL, Inc. · Class II
- TrueCPR™ Coaching Device — PHYSIO-CONTROL, 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
- Laerdal Medical Corp.
Sources (1)
- FDA UDI c4b8564d-101c-4087-8aa6-ac6c0bd71fad 36 fields · synced May 30, 2026