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Kroger

FDA UDI

Class II (US FDA UDI)

by MHC Medical Products

Identity

Trade Name
Kroger FDA UDI
Generic Name
Blood lancet, single-use FDA UDI
Device Name
Kroger Twist Lancets 26g FDA UDI
Model / Reference
926101 FDA UDI
Description
Kroger Twist Lancets 26g FDA UDI

Identifiers

Catalog Number
926101 FDA UDI
Primary DI / UDI-DI
MHC19261012 FDA UDI
FDA Product Code
FMK FDA UDI
GMDN Term
Blood lancet, single-use 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Blood lancet, single-use

Kroger by MHC Medical Products — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood lancet, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4a4d0d02-ac46-4225-894d-2ca48a28bc33 34 fields · synced May 31, 2026