Identity
- Trade Name
- Emergency Medical Products FDA UDI
- Generic Name
- Cardiopulmonary resuscitation kit, reusable FDA UDI
- Device Name
- Wisconsin First Responder Pediatric Kit FDA UDI
- Model / Reference
- WI-FR FDA UDI
- Description
- Wisconsin First Responder Pediatric Kit FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00851772007151 FDA UDI
- FDA Product Code
- BYG FDA UDICAN FDA UDIHTD FDA UDIGAX FDA UDIFMC FDA UDILDE FDA UDIMCY FDA UDIPHS FDA UDIDXQ FDA UDIBTM FDA UDIIMD FDA UDINOC FDA UDI
- GMDN Term
- Cardiopulmonary resuscitation kit, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5580 FDA UDI868.2700 FDA UDI878.4800 FDA UDI878.5900 FDA UDI880.6250 FDA UDI870.1875 FDA UDI880.5075 FDA UDI868.5110 FDA UDI870.1120 FDA UDI868.5915 FDA UDI890.5710 FDA UDI878.3910 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: First aid kit, medicatedAneroid manual sphygmomanometerMechanical external stethoscopeCardiopulmonary resuscitation kit, reusable
Emergency Medical Products by Emergency Medical Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 I | Pending data |
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Manufacturer
- Manufacturer
- Emergency Medical Products, Inc.
Sources (1)
- FDA UDI 12ec99df-5371-488a-bddc-3a1fc26763da 33 fields · synced May 30, 2026