Identity
- Trade Name
- inpen™ FDA UDI
- Generic Name
- Empty self-injector, mechanical FDA UDI
- Device Name
- KIT MMT-105ELBLNA INPEN ELI LILLY BLUE FDA UDI
- Model / Reference
- MMT-105ELBLNA FDA UDI
- Description
- KIT MMT-105ELBLNA INPEN ELI LILLY BLUE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00763000827151 FDA UDI
- 510(k) Number
- K201337 FDA UDI
- FDA Product Code
- NDC FDA UDIFMF FDA UDI
- GMDN Term
- Empty self-injector, mechanical FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 868.1890 FDA UDI880.5860 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.
- InPen Smart Insulin Delivery System — COMPANION MEDICAL, INC. · Class II
- HumatroPen® 6 mg — ELI LILLY AND COMPANY · Class II
- Genotropin Pen® 5 — Pharmacia & Upjohn Co. · Class II
- HumatroPen® 24 mg — ELI LILLY AND COMPANY · Class II
- Omnitrope® Pen 5 — Sandoz Inc. · Class II
- NovoPen Echo® — NOVO NORDISK INC. · Class II
- Omnitrope® Pen 10 — Sandoz Inc. · Class II
- InPen Smart Insulin System — COMPANION MEDICAL, INC. · Class II
Cleared under the same submission
K201337 also covers:
- InPen Smart Insulin Delivery System — COMPANION MEDICAL, INC.
- InPen Smart Insulin Delivery System — COMPANION MEDICAL, INC.
- InPen Smart Insulin System — COMPANION MEDICAL, INC.
- inpen™ — COMPANION MEDICAL, INC.
- inpen™ — COMPANION MEDICAL, INC.
- inpen™ — MEDTRONIC MINIMED, INC.
- inpen™ — MEDTRONIC MINIMED, INC.
- inpen™ — MEDTRONIC MINIMED, INC.
- inpen™ — MEDTRONIC MINIMED, INC.
- inpen™ — MEDTRONIC MINIMED, INC.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Medtronic Minimed, Inc.
Sources (1)
- FDA UDI 57169fa2-f50c-4485-9488-d1c735fe4958 35 fields · synced May 30, 2026