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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
36 Single head applicators packed as 4 sets of 9 single head applicators per set FDA UDI
Model / Reference
ST-9 8002 FDA UDI
Description
36 Single head applicators packed as 4 sets of 9 single head applicators per set FDA UDI

Identifiers

Catalog Number
ST-9 8002 FDA UDI
Primary DI / UDI-DI
B6828002 FDA UDI
510(k) Number
K172062 FDA UDI
FDA Product Code
LDH FDA UDI
GMDN Term
Allergy testing lancet FDA UDI

Classification

Commercial Distribution
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

Category: Allergy testing lancet

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

Similar devices

Also classified as Allergy testing lancet.

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 95206e99-1d32-40aa-b943-47f49b082b68 36 fields · synced Jun 1, 2026