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inpen™

FDA UDI

Class II (US FDA UDI)

by Medtronic Minimed, Inc.

Identity

Trade Name
inpen™ FDA UDI
Generic Name
Empty self-injector, mechanical FDA UDI
Device Name
KIT MMT-105ELGYNA INPEN ELI LILLY GREY FDA UDI
Model / Reference
MMT-105ELGYNA FDA UDI
Description
KIT MMT-105ELGYNA INPEN ELI LILLY GREY FDA UDI

Identifiers

Primary DI / UDI-DI
00763000827168 FDA UDI
510(k) Number
K201337 FDA UDI
FDA Product Code
FMF FDA UDI
NDC FDA UDI
GMDN Term
Empty self-injector, mechanical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5860 FDA UDI
868.1890 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Empty self-injector, mechanical

inpen™ by Medtronic Minimed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Empty self-injector, mechanical.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 88db7c34-c851-4dcc-b6d1-4144bfc86bb1 35 fields · synced May 30, 2026