Identity
- Trade Name
- Caterpillar FDA UDI
- Generic Name
- Non-neurovascular embolization plug, metallic FDA UDI
- Device Name
- Caterpillar Micro Arterial Embolization Device, 0.027 Inch ID Catheter Compatibility FDA UDI
- Model / Reference
- CTP027015U FDA UDI
- Description
- Caterpillar Micro Arterial Embolization Device, 0.027 Inch ID Catheter Compatibility FDA UDI
Identifiers
- Catalog Number
- CTP027015U FDA UDI
- Primary DI / UDI-DI
- 00801741155307 FDA UDI
- 510(k) Number
- K191532 FDA UDI
- FDA Product Code
- KRD FDA UDI
- GMDN Term
- Non-neurovascular embolization plug, metallic FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.3300 FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Caterpillar by ClearStream Technologies , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 II | Pending data |
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Manufacturer
- Manufacturer
- ClearStream Technologies , Ltd.
Sources (1)
- FDA UDI 3fb12492-2255-457f-8e61-89d271a1324a 38 fields · synced May 31, 2026