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JAS Diagnostics

FDA UDI

Class II (US FDA UDI)

by Drew Scientific , Ltd.

Identity

Trade Name
JAS Diagnostics FDA UDI
Generic Name
Urea IVD, control FDA UDI
Device Name
BUN LIQUID BULK (in 20L) FDA UDI
Model / Reference
BUN2-BUL FDA UDI
Description
BUN LIQUID BULK (in 20L) FDA UDI

Identifiers

Primary DI / UDI-DI
00817274021026 FDA UDI
FDA Product Code
CDQ FDA UDI
GMDN Term
Urea IVD, control FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1770 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Urea IVD, control

JAS Diagnostics by Drew Scientific , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Urea IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Drew Scientific , Ltd.

Sources (1)

  • FDA UDI 00bb06b7-26b5-4995-9fbc-2f36429cb280 35 fields · synced Jun 8, 2026