Identity
- Trade Name
- Kallestad FDA UDI
- Generic Name
- Mitochondrial antibody M2 (anti-Mi2) IVD, kit, enzyme immunoassay (EIA) FDA UDI
- Device Name
- Kallestad Anti-Mitochondrial Microplate EIA FDA UDI
- Model / Reference
- 31021 FDA UDI
- Description
- Kallestad Anti-Mitochondrial Microplate EIA FDA UDI
Identifiers
- Catalog Number
- 31021 FDA UDI
- Primary DI / UDI-DI
- 00847817016257 FDA UDI
- 510(k) Number
- K921183 FDA UDI
- FDA Product Code
- DBM FDA UDI
- GMDN Term
- Mitochondrial antibody M2 (anti-Mi2) IVD, kit, enzyme immunoassay (EIA) FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.5090 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
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
Yes
FDA UDI
Category: Mitochondrial antibody M2 (anti-Mi2) IVD, kit, enzyme immunoassay (EIA)
Kallestad by Bio-Rad Laboratories — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Mitochondrial antibody M2 (anti-Mi2) IVD, kit, enzyme immunoassay (EIA).
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- Trinity Biotech — CLARK LABORATORIES, INC. · Class II
- DIASTAT anti-Mitochondrial — Euro-Diagnostica AB · Class II
- QUANTA Lite® M2 EP (MIT3) ELISA Bulk Pack — INOVA DIAGNOSTICS, INC. · Class II
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
- Bio-Rad Laboratories
Sources (1)
- FDA UDI 9ec952fb-018c-4082-9afd-97d59702dd4d 38 fields · synced Jun 8, 2026