Identity
- Trade Name
- ResQPUMP ACD-CPR Device FDA UDI
- Generic Name
- Cardiac resuscitator, manual FDA UDI
- Device Name
- RESQPUMP ACD-CPD DEVICE FDA UDI
- Model / Reference
- 12-0823-000 FDA UDI
- Description
- RESQPUMP ACD-CPD DEVICE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00847946026950 FDA UDI
- FDA Product Code
- PIZ FDA UDI
- GMDN Term
- Cardiac resuscitator, manual FDA UDI
Classification
- Device Class
- Class III 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Cardiac resuscitator, manual
ResQPUMP ACD-CPR Device by Zoll Medical Corporation — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Cardiac resuscitator, manual.
- ResQCPR System — ADVANCED CIRCULATORY SYSTEMS INC · Class III
- Suction Cup, ACD-CPR Device — Zoll Medical Corporation · Class III
- ResQCPR System — Zoll Medical Corporation · Class III
- ResQPUMP International — Zoll Medical Corporation · Class III
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 III | Pending data |
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Manufacturer
- Manufacturer
- Zoll Medical Corporation
Sources (1)
- FDA UDI 497770ff-d4a5-4a70-b35d-92ab6ee6b2e3 34 fields · synced Jun 8, 2026