Identity
- Trade Name
- KBMED FDA UDI
- Generic Name
- Centrifuge tube IVD FDA UDI
- Device Name
- CENTRIFUGE TUBE, PP 15ML, PACK OF 100 FDA UDI
- Model / Reference
- CTPP15 FDA UDI
- Description
- CENTRIFUGE TUBE, PP 15ML, PACK OF 100 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00810100050528 FDA UDI
- FDA Product Code
- LXG FDA UDI
- GMDN Term
- Centrifuge tube IVD FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.2050 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
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: Centrifuge tube IVD
Kbmed by KB Medical (group), Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Centrifuge tube IVD.
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- Vivaspin Turbo 15 — SARTORIUS STEDIM LAB LIMITED · Class I
- Globe Scientific — GLOBE SCIENTIFIC, LLC · Class I
- KOVA — KOVA INTERNATIONAL INC · Class I
- KOVA — KOVA INTERNATIONAL INC · Class I
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
- KB Medical (group), Inc.
Sources (1)
- FDA UDI 1af04cec-bf6c-4833-893e-337e2d04bb84 33 fields · synced Jun 8, 2026