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Quintest® Multiple Skin Test Device

FDA UDI

by Jubilant Hollisterstier Llc

Identity

Trade Name
Quintest® Multiple Skin Test Device FDA UDI
Generic Name
Allergy testing lancet FDA UDI
Device Name
Multiple skin test system with 5 testing legs/tines FDA UDI
Model / Reference
8392ZA FDA UDI
Description
Multiple skin test system with 5 testing legs/tines FDA UDI

Identifiers

Catalog Number
8392ZA FDA UDI
Primary DI / UDI-DI
00365044000004 FDA UDI
510(k) Number
K953939 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

Yes

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

Yes

FDA UDI

Category: Allergy testing lancet

Quintest® Multiple Skin Test Device by Jubilant Hollisterstier Llc — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Allergy testing lancet.

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 d3af4dfe-f0b4-451e-9c56-72e153730cff 36 fields · synced Jun 7, 2026