Identity
- Trade Name
- Genesis RapidWeld STW Sterile Tube Welder FDA UDI
- Generic Name
- Laboratory tubing welder FDA UDI
- Device Name
- The Genesis Rapid Weld STW is a medical device used in laboratories, designed for the purpose of making sterile connections in PVC tubing in blood processing applications. The device enables fluid transfer while maintaining a closed system without the need for a consumable (disposable wafer). FDA UDI
- Model / Reference
- GRW-430 FDA UDI
- Description
- The Genesis Rapid Weld STW is a medical device used in laboratories, designed for the purpose of making sterile connections in PVC tubing in blood processing applications. The device enables fluid transfer while maintaining a closed system without the need for a consumable (disposable wafer). FDA UDI
Identifiers
- Catalog Number
- 480-RW-2607-00 FDA UDI
- Primary DI / UDI-DI
- 00866305000202 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
Yes
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Weight — 2.5 Kilogram FDA UDIWidth — 14.2 Centimeter FDA UDIHeight — 9.9 Centimeter FDA UDILength — 33 Centimeter FDA UDI
Category: Laboratory tubing welder
Genesis RapidWeld STW Sterile Tube Welder by Genesisbps Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Laboratory tubing welder.
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- Genesis RapidWeld II STW Sterile Tube Welder — GENESISBPS LLC · Class II
- RapidWeld Blade Module Kit — GENESISBPS LLC · Class II
- TCD B40 Wafers — GENESISBPS LLC · Class II
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- Total Containment Device (TCD) — GENESISBPS LLC · Class II
Cleared under the same submission
BK140187 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Genesisbps Llc
Sources (1)
- FDA UDI 83533c16-a519-4c31-930e-26ae04ab520a 38 fields · synced May 30, 2026