← Back to catalogue

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™ 52 FDA UDI

Identifiers

Catalog Number
55060 FDA UDI
Primary DI / UDI-DI
07350096321606 FDA UDI
510(k) Number
K143445 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

No

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.

Cleared under the same submission

K143445 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Integration Diagnostics Sweden AB

Sources (1)

  • FDA UDI 3edf6055-f2c0-4d0f-8993-4b6e859eaeba 34 fields · synced May 30, 2026