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Quidel Molecular

FDA UDI

Class I (US FDA UDI)

by Diagnostic Hybrids, Inc.

Identity

Trade Name
Quidel Molecular FDA UDI
Generic Name
Beta-haemolytic Group B Streptococcus nucleic acid IVD, control FDA UDI
Device Name
QMol GBS Control Set FDA UDI
Model / Reference
M116 FDA UDI
Description
QMol GBS Control Set FDA UDI

Identifiers

Catalog Number
M116 FDA UDI
Primary DI / UDI-DI
30014613311164 FDA UDI
FDA Product Code
JJX FDA UDI
GMDN Term
Beta-haemolytic Group B Streptococcus nucleic acid 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

Yes

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: Beta-haemolytic Group B Streptococcus nucleic acid IVD, control

Quidel Molecular by Diagnostic Hybrids, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Beta-haemolytic Group B Streptococcus nucleic acid IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5738e990-6095-4f0f-bbf8-5e3bd35e1f15 35 fields · synced May 30, 2026