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Skin Test Reservoirs

FDA UDI

by Jubilant Hollisterstier Llc

Identity

Trade Name
Skin Test Reservoirs FDA UDI
Generic Name
Allergy testing lancet FDA UDI
Device Name
Holds testing antigens FDA UDI
Model / Reference
8924ZA FDA UDI
Description
Holds testing antigens FDA UDI

Identifiers

Catalog Number
8924ZA FDA UDI
Primary DI / UDI-DI
00365044000042 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

No

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

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

Skin Test Reservoirs 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 2e692268-e62a-40f8-9c7a-509252f96c1c 36 fields · synced Jun 8, 2026