FDA UDI In Commercial Distribution 🇺🇸 United States

Omnipod 5 Pod

DI: 10385083000411 · Model: POD-OMNI-I1-6220 · Insulet Corporation
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Omnipod 5 Pod
Primary DI
10385083000411
Version / Model
POD-OMNI-I1-6220
Company Name
Insulet Corporation
Labeler DUNS
051334402
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-04
Public Version
1
Public Version Date
2025-12-12
Public Version Status
New
Public Device Record Key
60548b36-10f9-47ac-87c0-2a11704d6daf

Device Description

Omnipod 5 Pod

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
QFG Alternate Controller Enabled Insulin Infusion Pump
QJI Interoperable Automated Glycemic Controller

GMDN Terms

Code Name
60770 Ambulatory insulin infusion pump/interstitial glucose monitoring system

Identifiers

Type ID
Package 20385083000425
Primary 10385083000411

Customer Contacts