Identity
- Trade Name
- ABBOTT FDA UDI
- Generic Name
- Methotrexate therapeutic drug monitoring IVD, kit, chemiluminescent immunoassay FDA UDI
- Device Name
- XSYSTEMS TDx/TDx Flx Methotrexate II Reagent Pack FDA UDI
- Model / Reference
- 7A12-60 FDA UDI
- Description
- XSYSTEMS TDx/TDx Flx Methotrexate II Reagent Pack FDA UDI
Identifiers
- Catalog Number
- 07A1260 FDA UDI
- Primary DI / UDI-DI
- 00380740011635 FDA UDI
- FDA Product Code
- LAO FDA UDI
- GMDN Term
- Methotrexate therapeutic drug monitoring IVD, kit, chemiluminescent immunoassay FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- Not 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
Yes
FDA UDI
Over-the-Counter
No
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Abbott by Abbott Laboratories, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 U | Pending data |
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Manufacturer
- Manufacturer
- Abbott Laboratories, Inc.
Sources (1)
- FDA UDI f07ed665-114f-4854-bc56-30f63aceb84f 37 fields · synced Jun 1, 2026