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metene S BLOOD GLUCOSE MONITORING SYSTEM

FDA UDI

Class II (US FDA UDI)

by Metene Limited

Identity

Trade Name
metene S BLOOD GLUCOSE MONITORING SYSTEM FDA UDI
Generic Name
Glucose analyser IVD, home-use FDA UDI
Device Name
Lancet 50 Pcs Strip 50 Pcs Control solution 1 Bottle Lancing device 1 Pcs FDA UDI
Model / Reference
S FDA UDI
Description
Lancet 50 Pcs Strip 50 Pcs Control solution 1 Bottle Lancing device 1 Pcs FDA UDI

Identifiers

Primary DI / UDI-DI
00850063675680 FDA UDI
510(k) Number
K061181 FDA UDI
FDA Product Code
NBW FDA UDI
GMDN Term
Glucose analyser IVD, home-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1345 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Glucose analyser IVD, home-use

metene S BLOOD GLUCOSE MONITORING SYSTEM by Metene Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Glucose analyser IVD, home-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Metene Limited

Sources (1)

  • FDA UDI 218c1bb0-471a-4a64-922e-095ef3f338e7 34 fields · synced Jun 8, 2026