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Jj Care

FDA UDI

Class II (US FDA UDI)

by Jack Jack Llc

Identity

Trade Name
JJ CARE FDA UDI
Generic Name
Manual blood lancing device, reusable FDA UDI
Device Name
Lancing Device- People with diabetes may use a lancet to test and monitor their blood glucose levels. Regular testing can help people manage their diabetes symptoms. FDA UDI
Model / Reference
HH-X-T FDA UDI
Description
Lancing Device- People with diabetes may use a lancet to test and monitor their blood glucose levels. Regular testing can help people manage their diabetes symptoms. FDA UDI

Identifiers

Primary DI / UDI-DI
15060988910038 FDA UDI
FDA Product Code
QRK FDA UDI
GMDN Term
Manual blood lancing device, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4850 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Manual blood lancing device, reusable

Jj Care by Jack Jack Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual blood lancing device, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Jack Jack Llc

Sources (1)

  • FDA UDI 8350272f-ded1-439b-a7c3-49c3f1369070 35 fields · synced May 30, 2026