Identity
- Trade Name
- Beaty FDA UDI
- Generic Name
- Cardiopulmonary resuscitation feedback device, electronic FDA UDI
- Model / Reference
- BE8789US FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07290017875002 FDA UDI
- FDA Product Code
- PMJ 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
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Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
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HCT/P
No
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Premarket Exempt
Yes
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Lot / Batch Number
Yes
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Serial Number
No
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Expiration Date
No
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Manufacturing Date
Yes
FDA UDI
Category: Cardiopulmonary resuscitation feedback device, electronic
Beaty by Medical Feedback Technologies Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cardiopulmonary resuscitation feedback device, electronic.
- TrueCPR™ Coaching Device — PHYSIO-CONTROL, Inc. · Class II
- TrueCPR™ Coaching Device — PHYSIO-CONTROL, Inc. · Class II
- CPRmeter 2 (Multi-bundle) — Laerdal Medical Corp. · 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
- Medical Feedback Technologies Ltd
Sources (1)
- FDA UDI c5fdc501-015f-4573-8fd5-6d79d5e77901 32 fields · synced May 30, 2026