Identity
- Trade Name
- UMS Universal Tube/Cap FDA UDI
- Generic Name
- Centrifuge tube IVD FDA UDI
- Device Name
- Universal Tube FDA UDI
- Model / Reference
- US0101QD FDA UDI
- Description
- Universal Tube FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00892159002123 FDA UDI
- FDA Product Code
- NNK FDA UDI
- GMDN Term
- Centrifuge tube IVD FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.3250 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Centrifuge tube IVD
UMS Universal Tube/Cap by Typenex Medical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Centrifuge tube IVD.
- KBMED — KB Medical (group), Inc. · Class I
- Vivafree 2 — SARTORIUS STEDIM LAB LIMITED · Class I
- KOVA — KOVA INTERNATIONAL INC · Class I
- KOVA — KOVA INTERNATIONAL INC · Class I
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class I
- Vivaspin Turbo 15 — SARTORIUS STEDIM LAB LIMITED · Class I
- Globe Scientific — GLOBE SCIENTIFIC, LLC · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Typenex Medical, LLC
Sources (1)
- FDA UDI 7f20c72e-c611-45ac-8699-5a0f596a50ae 33 fields · synced May 30, 2026