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Drew Scientific

FDA UDI

Class I (US FDA UDI)

by Drew Scientific , Ltd.

Identity

Trade Name
Drew Scientific FDA UDI
Generic Name
Immunohistochemistry antibody diluent IVD FDA UDI
Device Name
EX ISO Diff Diluent 20L FDA UDI
Model / Reference
RA-1720 FDA UDI
Description
EX ISO Diff Diluent 20L FDA UDI

Identifiers

Primary DI / UDI-DI
00817274020456 FDA UDI
FDA Product Code
GIF FDA UDI
GMDN Term
Immunohistochemistry antibody diluent IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.8200 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

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: Immunohistochemistry antibody diluent IVD

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

Similar devices

Also classified as Immunohistochemistry antibody diluent IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 27b7c9ee-f268-4d11-a781-d8b34562b308 35 fields · synced Jun 1, 2026