Identity
- Trade Name
- CPR4 FDA UDI
- Generic Name
- Cardiac pulse generator programmer FDA UDI
- Device Name
- Inductive Telemetry Head CPR4 USB FDA UDI
- Model / Reference
- B10031 FDA UDI
- Description
- Inductive Telemetry Head CPR4 USB FDA UDI
Identifiers
- Catalog Number
- B10031 FDA UDI
- Primary DI / UDI-DI
- 08031527019611 FDA UDI
- PMA Number
- P980049 FDA UDI
- FDA Product Code
- MRM FDA UDI
- GMDN Term
- Cardiac pulse generator programmer 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
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: Cardiac pulse generator programmer
Cpr4 by Microport Crm Srl — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
P980049 also covers:
- CPR3H — MICROPORT CRM SRL
- Intensia — MICROPORT CRM SRL
- Intensia — MICROPORT CRM SRL
- PLATINIUM — MICROPORT CRM SRL
- PLATINIUM — MICROPORT CRM SRL
- PLATINIUM — MICROPORT CRM SRL
- PLATINIUM — MICROPORT CRM SRL
- Paradym RF — MICROPORT CRM SRL
- Paradym RF — MICROPORT CRM SRL
- RMS — MICROPORT CRM SRL
- SMARTVIEW — MICROPORT CRM SRL
- SMARTVIEW — MICROPORT CRM SRL
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Microport Crm Srl
Sources (1)
- FDA UDI 334c140d-2726-426b-815b-bba4aeeeaece 35 fields · synced May 30, 2026