Identity
- Trade Name
- CompoDock FDA UDI
- Generic Name
- Laboratory tubing welder FDA UDI
- Device Name
- The CompoDock is used for the production of special cellular blood components, e.g. in blood banks where tube connections are needed that provide protection against microbial contamination. The CompoDock is a high-frequency connection device that permits sterile connection of medical PVC tubes to one another. Here, sterile connection is achieved when germs from the environment are prevented from being carried into the closed systems. The closed system is maintained after the docking process. FDA UDI
- Model / Reference
- 9028721 FDA UDI
- Description
- The CompoDock is used for the production of special cellular blood components, e.g. in blood banks where tube connections are needed that provide protection against microbial contamination. The CompoDock is a high-frequency connection device that permits sterile connection of medical PVC tubes to one another. Here, sterile connection is achieved when germs from the environment are prevented from being carried into the closed systems. The closed system is maintained after the docking process. FDA UDI
Identifiers
- Catalog Number
- 9028721 FDA UDI
- Primary DI / UDI-DI
- 04086000860215 FDA UDI
- FDA Product Code
- KSB FDA UDI
- GMDN Term
- Laboratory tubing welder FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.9875 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Laboratory tubing welder
CompoDock by Fresenius Kabi — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Laboratory tubing welder.
- Genesis RapidWeld II STW Sterile Tube Welder — GENESISBPS LLC · Class II
- RapidWeld Blade Module Kit — GENESISBPS LLC · Class II
- BMS — Wuhan BMS Medicaltech Co., Ltd · Class II
- TCD B40 Wafers — GENESISBPS LLC · Class II
- RapidWeld Blade Module Kit — GENESISBPS LLC · Class II
- Total Containment Device (TCD) — GENESISBPS LLC · Class II
- Genesis RapidWeld STW Sterile Tube Welder — GENESISBPS LLC · Class II
- RapidWeld Blade Module Kit — GENESISBPS LLC · Class II
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Fresenius Kabi
Sources (1)
- FDA UDI 6acfbf22-f04b-43a2-9c26-b4ca67900e51 36 fields · synced Jun 8, 2026