Identity
- Trade Name
- DUPLOCATH FDA UDI
- Generic Name
- Open-surgery adhesive/sealant applicator, dual-channel FDA UDI
- Device Name
- Catheter for the simultaneous application of Baxter's two-component fibrin sealant in areas of the operation site where access is difficult. The Application of Baxter's two-component fibrin sealant can be carried out via a double syringe system and the two-lumen Duplocath application catheter FDA UDI
- Model / Reference
- 1506165 FDA UDI
- Description
- Catheter for the simultaneous application of Baxter's two-component fibrin sealant in areas of the operation site where access is difficult. The Application of Baxter's two-component fibrin sealant can be carried out via a double syringe system and the two-lumen Duplocath application catheter FDA UDI
Identifiers
- Catalog Number
- 1506165 FDA UDI
- Primary DI / UDI-DI
- 00085412600024 FDA UDI
- FDA Product Code
- FMF FDA UDI
- GMDN Term
- Open-surgery adhesive/sealant applicator, dual-channel FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5860 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Length — 25 Centimeter FDA UDI
Category: Open-surgery adhesive/sealant applicator, dual-channel
Duplocath by Baxter International Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Open-surgery adhesive/sealant applicator, dual-channel.
- DUPLOTIP — Micromedics, Inc. · Class II
- PREVELEAK SURGICAL SEALANT — Baxter Healthcare Corp · Class III
- Gasless Tip — Micromedics, Inc. · Class II
- DUPLOTIP — Micromedics, Inc. · Class II
- FibriJet — Micromedics, Inc. · Class I
- Pramand — Micromedics, Inc. · Class II
- DUPLOTIP — Micromedics, Inc. · Class II
- Coseal Surgical Sealant Extended Applicator — Baxter Healthcare Corp · Class III
Cleared under the same submission
BK170033 also covers:
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
- Baxter International Inc.
Sources (1)
- FDA UDI 96b43f6d-247a-495b-91d0-baf3691f2bc9 38 fields · synced May 30, 2026