Identity
- Trade Name
- CODMAN® BACTISEAL® FDA UDI
- Generic Name
- Peritoneal/atrial cerebrospinal fluid catheter FDA UDI
- Device Name
- CODMAN® BACTISEAL® Clear with Barium Stripe Catheter Kit FDA UDI
- Model / Reference
- NS0340 FDA UDI
- Description
- CODMAN® BACTISEAL® Clear with Barium Stripe Catheter Kit FDA UDI
Identifiers
- Catalog Number
- NS0340 FDA UDI
- Primary DI / UDI-DI
- 10381780524076 FDA UDI
- FDA Product Code
- HCA FDA UDI
- GMDN Term
- Peritoneal/atrial cerebrospinal fluid catheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.4100 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
Yes
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
Dimensions & Sizes
- Size
- Length — 15 Centimeter FDA UDILength — 120 Centimeter FDA UDI
Category: Intracerebral infusion/drainage catheter, long-termPeritoneal/atrial cerebrospinal fluid catheter
Codman® Bactiseal® by Integra LifeSciences Production Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 II | Pending data |
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Manufacturer
- Manufacturer
- Integra LifeSciences Production Corporation
Sources (1)
- FDA UDI 91a742c1-77b0-4af1-a8d2-7cc8dd0a4698 37 fields · synced Jun 9, 2026