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StatFax

FDA UDI

Class I (US FDA UDI)

by Awareness Technology, Incorporated

Identity

Trade Name
StatFax FDA UDI
Generic Name
Microplate washer IVD FDA UDI
Device Name
Digital Dry Bath FDA UDI
Model / Reference
2600 FDA UDI
Description
Digital Dry Bath FDA UDI

Identifiers

Primary DI / UDI-DI
00850229007072 FDA UDI
FDA Product Code
JTQ FDA UDI
GMDN Term
Microplate washer IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
866.2540 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Microplate washer IVD

StatFax by Awareness Technology, Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microplate washer IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 16826501-fd25-467c-a9e4-82aaefef6e53 33 fields · synced Jun 8, 2026