Identity
- Trade Name
- MeDiCa FDA UDI
- Generic Name
- Mitochondrial antibody M2 (anti-Mi2) IVD, kit, fluorescent immunoassay FDA UDI
- Device Name
- Rat Kidney 8 Well Slide (each) FDA UDI
- Model / Reference
- 0302 FDA UDI
- Description
- Rat Kidney 8 Well Slide (each) FDA UDI
Identifiers
- Catalog Number
- 0302 FDA UDI
- Primary DI / UDI-DI
- 00813545026615 FDA UDI
- 510(k) Number
- K790295 FDA UDI
- FDA Product Code
- DBM FDA UDI
- GMDN Term
- Mitochondrial antibody M2 (anti-Mi2) IVD, kit, fluorescent immunoassay 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
No
FDA UDI
Category: Mitochondrial antibody M2 (anti-Mi2) IVD, kit, fluorescent immunoassay
MeDiCa by Scimedx Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Histofluor® Rodent LKS Fluorescent Antibody Test System — IMMUNO CONCEPTS INC
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Cleared under the same submission
K790295 also covers:
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Scimedx Corp.
Sources (1)
- FDA UDI d1b5da02-a6ba-493c-bb01-9f2d72acf52d 36 fields · synced May 30, 2026