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Legionella DFA Mounting Medium

FDA UDI

Class II (US FDA UDI)

by Pro-Lab, Incorporated

Identity

Trade Name
Legionella DFA Mounting Medium FDA UDI
Generic Name
Microscopy mounting medium IVD FDA UDI
Device Name
Mounting Medium FDA UDI
Model / Reference
PL.213 FDA UDI
Description
Mounting Medium FDA UDI

Identifiers

Catalog Number
PL.213 FDA UDI
Primary DI / UDI-DI
10628429001742 FDA UDI
FDA Product Code
LHL FDA UDI
GMDN Term
Microscopy mounting medium IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3300 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

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: Microscopy mounting medium IVD

Legionella DFA Mounting Medium by Pro-Lab, Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microscopy mounting medium IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pro-Lab, Incorporated

Sources (1)

  • FDA UDI f4b983ad-e9bf-4827-bf8d-d58d373ffcf3 34 fields · synced Jun 8, 2026