Identity
- Trade Name
- Multi-Sampling Connector FDA UDI
- Generic Name
- Luer-ended blood collection tube spike FDA UDI
- Device Name
- Semi-Assembled Multi-Sample Access Device. FDA UDI
- Model / Reference
- 4R5129 FDA UDI
- Description
- Semi-Assembled Multi-Sample Access Device. FDA UDI
Identifiers
- Catalog Number
- 4R5129 FDA UDI
- Primary DI / UDI-DI
- 04086000101240 FDA UDI
- FDA Product Code
- KST FDA UDI
- GMDN Term
- Luer-ended blood collection tube spike FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.9125 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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Luer-ended blood collection tube spike
Multi-Sampling Connector by Fresenius Kabi — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Fresenius Kabi
Sources (1)
- FDA UDI 4d533052-2935-497d-864e-32b9acb29f90 35 fields · synced Jun 1, 2026