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AllergiEnd ST-9

FDA UDI

by Medscience Research Group, Inc.

Identity

Trade Name
AllergiEnd ST-9 FDA UDI
Generic Name
General laboratory assay tray FDA UDI
Device Name
36 Well Test Tray FDA UDI
Model / Reference
1001-36 FDA UDI
Description
36 Well Test Tray FDA UDI

Identifiers

Catalog Number
1001-36 FDA UDI
Primary DI / UDI-DI
B6821001360 FDA UDI
510(k) Number
K172062 FDA UDI
FDA Product Code
LDH FDA UDI
GMDN Term
General laboratory assay tray FDA UDI

Classification

Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

AllergiEnd ST-9 by Medscience Research Group, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2923802c-d67d-409d-90f5-4a40396ddca0 38 fields · synced May 30, 2026