Identity
- Trade Name
- ALT Reagent FDA UDI
- Generic Name
- Alanine aminotransferase (ALT) IVD, kit, enzyme spectrophotometry FDA UDI
- Device Name
- For the quantitative in vitro determination of Alanine Aminotransferase (ALT) in serum and plasma. 6 x 51 ml, 6 x 14 ml FDA UDI
- Model / Reference
- ALT505 FDA UDI
- Description
- For the quantitative in vitro determination of Alanine Aminotransferase (ALT) in serum and plasma. 6 x 51 ml, 6 x 14 ml FDA UDI
Identifiers
- Catalog Number
- ALT505 FDA UDI
- Primary DI / UDI-DI
- 00817439020161 FDA UDI
- FDA Product Code
- CKA FDA UDI
- GMDN Term
- Alanine aminotransferase (ALT) IVD, kit, enzyme spectrophotometry FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 862.1030 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
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
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: Alanine aminotransferase (ALT) IVD, kit, enzyme spectrophotometry
ALT Reagent by Medtest DX — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Alanine aminotransferase (ALT) IVD, kit, enzyme spectrophotometry.
- ALT/SGPT Liqui-UV® — STANBIO LABORATORY, L.P. · Class I
- ALT — Randox Laboratories, Ltd. · Class I
- ALT R1 (w/ssa#) — POINTE SCIENTIFIC, INC. · Class I
- ABX PENTRA ALT CP — Horiba Abx · Class I
- Alanine Aminotransferase acc. to IFCC with pyridoxal phosphate activation — Roche Diagnostics Corp. · Class I
- ALANINE AMINOTRANSFERASE (ALT) — Randox Laboratories, Ltd. · Class I
- Alanine Aminotransferase / Aspartate Aminotransferase acc. to IFCC with PYP — Roche Diagnostics Corp. · Class I
- ALT R1 (w/ssa#) — POINTE SCIENTIFIC, 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
- Medtest DX
Sources (1)
- FDA UDI 29842098-2962-41c9-a533-42e24c94444e 36 fields · synced May 30, 2026