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ketodoc Blood Glucose Plus B-Ketone Monitoring System

FDA UDI

Class II (US FDA UDI)

by Rediston Limited

Identity

Trade Name
ketodoc Blood Glucose Plus B-Ketone Monitoring System FDA UDI
Generic Name
Multiple clinical chemistry analyte monitoring system IVD, home-use FDA UDI
Device Name
Lancing device*1 Lancet*20pcs Blood glucose test strip*10pcs Ketone test strip*10pcs FDA UDI
Model / Reference
TD-4141 FDA UDI
Description
Lancing device*1 Lancet*20pcs Blood glucose test strip*10pcs Ketone test strip*10pcs FDA UDI

Identifiers

Primary DI / UDI-DI
00703674534436 FDA UDI
FDA Product Code
NBW FDA UDI
GMDN Term
Multiple clinical chemistry analyte monitoring system 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: Multiple clinical chemistry analyte monitoring system IVD, home-use

ketodoc Blood Glucose Plus B-Ketone Monitoring System by Rediston Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple clinical chemistry analyte monitoring system IVD, home-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Rediston Limited

Sources (1)

  • FDA UDI 178ea783-053f-40d6-a1ca-d8057bac524a 33 fields · synced Jun 1, 2026