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St-9

FDA UDI

by Medscience Research Group, Inc.

Identity

Trade Name
ST-9 FDA UDI
Generic Name
Allergy testing lancet FDA UDI
Device Name
Asymmetric Multiple Skin Testing Device for Percutaneous Skin Testing, 12 applicators individually package and sold as a unit of 12 applicators. FDA UDI
Model / Reference
ST-9 1000-12 FDA UDI
Description
Asymmetric Multiple Skin Testing Device for Percutaneous Skin Testing, 12 applicators individually package and sold as a unit of 12 applicators. FDA UDI

Identifiers

Catalog Number
ST-9 1000-12 FDA UDI
Primary DI / UDI-DI
B682100012 FDA UDI
510(k) Number
K172062 FDA UDI
FDA Product Code
LDH FDA UDI
GMDN Term
Allergy testing lancet FDA UDI

Classification

Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

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

Cleared under the same submission

K172062 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medscience Research Group, Inc.

Sources (1)

  • FDA UDI 56522603-959b-4008-9ff9-483730b13b86 38 fields · synced Jun 1, 2026