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Jac-cell Medic

FDA UDI

Class II (US FDA UDI)

by 9001-2030 Québec Inc

Identity

Trade Name
Jac-cell Medic FDA UDI
Generic Name
Multi-parameter device tester FDA UDI
Device Name
Insulation Tester FDA UDI
Model / Reference
ATI-021 FDA UDI
Description
Insulation Tester FDA UDI

Identifiers

Primary DI / UDI-DI
B460ATI0210 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Multi-parameter device tester FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Weight — 0.51 Pound FDA UDI
Depth — 1.2 Inch FDA UDI
Width — 3.5 Inch FDA UDI
Height — 6 Inch FDA UDI

Category: Multi-parameter device tester

Jac-cell Medic by 9001-2030 Québec Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-parameter device tester.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
9001-2030 Québec Inc

Sources (1)

  • FDA UDI 86bdecd3-97b8-431c-9c20-7f0941bff235 34 fields · synced May 30, 2026