← Back to catalogue

PreciControl Toxo IgG

FDA UDI

Class I (US FDA UDI)

by Roche Diagnostics Corp.

Identity

Trade Name
PreciControl Toxo IgG FDA UDI
Generic Name
Toxoplasma gondii immunoglobulin G (IgG) antibody IVD, control FDA UDI
Model / Reference
4618823160 FDA UDI

Identifiers

Catalog Number
4618823160 FDA UDI
Primary DI / UDI-DI
04015630939343 FDA UDI
FDA Product Code
JJX FDA UDI
GMDN Term
Toxoplasma gondii immunoglobulin G (IgG) antibody IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 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

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

Category: Toxoplasma gondii immunoglobulin G (IgG) antibody IVD, control

PreciControl Toxo IgG by Roche Diagnostics Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Toxoplasma gondii immunoglobulin G (IgG) antibody IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI c3627eac-6398-4808-bbbb-80f4a65f88c2 33 fields · synced May 30, 2026