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Easy Plus II

FDA UDI

Class I (US FDA UDI)

by Biotest Medical Corporation

Identity

Trade Name
Easy Plus II FDA UDI
Generic Name
Glucose analyser IVD, home-use/point-of-care, line-powered FDA UDI
Device Name
Easy Plus II Blood Glucose Monitoring System 6276-S FDA UDI
Model / Reference
6276-S(BZG60276HA) FDA UDI
Description
Easy Plus II Blood Glucose Monitoring System 6276-S FDA UDI

Identifiers

Primary DI / UDI-DI
04719871820056 FDA UDI
FDA Product Code
JJX FDA UDI
CGA FDA UDI
NBW FDA UDI
GMDN Term
Glucose analyser IVD, home-use/point-of-care, line-powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 FDA UDI
862.1345 FDA UDI
Commercial Distribution
Not 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

Yes

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

Easy Plus II by Biotest Medical Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1b4e6734-6d7d-4a91-bd5e-49454da11d14 34 fields · synced May 30, 2026