Identity
- Trade Name
- CODMAN FDA UDI
- Generic Name
- Implantable intrathecal infusion pump, nonprogrammable FDA UDI
- Device Name
- Constant Flow Implantable Pump With Bolus Safety Valve and Operating Room Prep Kit FDA UDI
- Model / Reference
- AP-03000UL FDA UDI
- Description
- Constant Flow Implantable Pump With Bolus Safety Valve and Operating Room Prep Kit FDA UDI
Identifiers
- Catalog Number
- AP03000UL FDA UDI
- Primary DI / UDI-DI
- 10886704043621 FDA UDI
- PMA Number
- P890055 FDA UDI
- FDA Product Code
- LKK FDA UDI
- GMDN Term
- Implantable intrathecal infusion pump, nonprogrammable FDA UDI
Classification
- Device Class
- Class III 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Codman by Cerenovus, Inc. — Class III — 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 III | Pending data |
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Manufacturer
- Manufacturer
- Cerenovus, Inc.
Sources (1)
- FDA UDI 1859570c-e181-41b1-8701-31d469dc8cb9 38 fields · synced Jun 8, 2026