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Chlamydia Antigen Control Slide, 2 wells

FDA UDI

Class I (US FDA UDI)

by Bion Enterprises, Ltd.

Identity

Trade Name
Chlamydia Antigen Control Slide, 2 wells FDA UDI
Generic Name
Multiple Chlamydia species antigen IVD, control FDA UDI
Model / Reference
QCH-4102 FDA UDI

Identifiers

Catalog Number
QCH-4102 FDA UDI
Primary DI / UDI-DI
B110QCH41020 FDA UDI
510(k) Number
K890616 FDA UDI
FDA Product Code
LJG FDA UDI
GMDN Term
Multiple Chlamydia species antigen IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2660 FDA UDI
Commercial Distribution
Not 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Chlamydia Antigen Control Slide, 2 wells by Bion Enterprises, Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6e45fbea-3403-4ac5-92c4-ec6278278085 37 fields · synced May 30, 2026