Identity
- Trade Name
- ARK™ Methylphenidate Negative Calibrator FDA UDI
- Generic Name
- Amphetamine/methamphetamine group IVD, calibrator FDA UDI
- Device Name
- ARK™ Methylphenidate Metabolite Negative Calibrator is intended for use in calibration of the ARK™ Methylphenidate Metabolite Assay. FDA UDI
- Model / Reference
- 5042-0002-01 FDA UDI
- Description
- ARK™ Methylphenidate Metabolite Negative Calibrator is intended for use in calibration of the ARK™ Methylphenidate Metabolite Assay. FDA UDI
Identifiers
- Catalog Number
- 5042-0002-01 FDA UDI
- Primary DI / UDI-DI
- 00858724003575 FDA UDI
- FDA Product Code
- DLJ FDA UDI
- GMDN Term
- Amphetamine/methamphetamine group IVD, calibrator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.3200 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
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
Category: Amphetamine/methamphetamine group IVD, calibrator
ARK™ Methylphenidate Negative Calibrator by Ark Diagnostics Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Amphetamine/methamphetamine group IVD, calibrator.
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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 II | Pending data |
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Manufacturer
- Manufacturer
- Ark Diagnostics Inc
Sources (1)
- FDA UDI 1cdd8e7f-3539-46ed-b294-e294fc90a30c 36 fields · synced May 30, 2026