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MulTipeg™

FDA UDI

Class I (US FDA UDI)

by Integration Diagnostics Sweden AB

Identity

Trade Name
MulTipeg™ FDA UDI
Generic Name
Multimeter FDA UDI
Model / Reference
MulTipeg™ 107 FDA UDI

Identifiers

Catalog Number
55141 FDA UDI
Primary DI / UDI-DI
07350096322276 FDA UDI
FDA Product Code
EKX FDA UDI
GMDN Term
Multimeter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4200 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

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Multimeter

MulTipeg™ by Integration Diagnostics Sweden AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multimeter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Integration Diagnostics Sweden AB

Sources (1)

  • FDA UDI 81be3b33-1765-4650-86cb-7d5422f82cee 33 fields · synced May 30, 2026