Identity
- Trade Name
- ANTI-TOXOPLASMA GONDII FDA UDI
- Generic Name
- Toxoplasma gondii total antibody IVD, reagent FDA UDI
- Model / Reference
- PU125-5UP FDA UDI
Identifiers
- Catalog Number
- PU125-5UP FDA UDI
- Primary DI / UDI-DI
- 00810119674425 FDA UDI
- FDA Product Code
- MVU FDA UDI
- GMDN Term
- Toxoplasma gondii total antibody IVD, reagent FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.4020 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
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
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
Dimensions & Sizes
- Size
- Total Volume — 0.5 Milliliter FDA UDI
Category: Toxoplasma gondii total antibody IVD, reagent
Anti-Toxoplasma Gondii by Biogenex Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Toxoplasma gondii total antibody IVD, reagent.
- ANTI-TOXOPLASMA — Biogenex Laboratories, 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
- Biogenex Laboratories, Inc.
Sources (1)
- FDA UDI 0e6f3b36-794a-4c2a-985b-84af2136016d 36 fields · synced May 30, 2026