Identity
- Trade Name
- Intica Neo 5 DR-T DF-1 ProMRI FDA UDI
- Generic Name
- Dual-chamber implantable defibrillator FDA UDI
- Model / Reference
- 429568 FDA UDI
Identifiers
- Catalog Number
- 429568 FDA UDI
- Primary DI / UDI-DI
- 04035479156947 FDA UDI
- FDA Product Code
- MRM FDA UDI
- GMDN Term
- Dual-chamber implantable defibrillator FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Category: Dual-chamber implantable defibrillator
Intica Neo 5 DR-T DF-1 ProMRI by BIOTRONIK SE & Co. KG — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Dual-chamber implantable defibrillator.
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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 III | Pending data |
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Manufacturer
- Manufacturer
- BIOTRONIK SE & Co. KG
Sources (1)
- FDA UDI 391fb618-7fca-4e33-98d6-a083a1d22bd8 35 fields · synced May 29, 2026