Identity
- Trade Name
- SMARTVIEW FDA UDI
- Generic Name
- Cardiac pulse generator programmer FDA UDI
- Model / Reference
- 2.52 UG1 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08031527016788 FDA UDI
- PMA Number
- P980049 FDA UDI
- FDA Product Code
- NVZ 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Cardiac pulse generator programmer
Smartview 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
- CPR4 — 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
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
- Microport Crm Srl
Sources (1)
- FDA UDI 7eec29d9-968e-4a2d-8848-44da72a62b0a 33 fields · synced May 30, 2026