FDA UDI In Commercial Distribution 🇺🇸 United States

iLet Flex

DI: 05705244027206 · Model: FG000063-11 · Unomedical A/S
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
iLet Flex
Primary DI
05705244027206
Version / Model
FG000063-11
Company Name
Unomedical A/S
Labeler DUNS
306032491
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-14
Public Version
1
Public Version Date
2025-12-22
Public Version Status
New
Public Device Record Key
9d8cf43f-8c62-4640-a01f-0af1377f892a

Device Description

ilet Flex, 9mm, 80cm 2 pack

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
Labeling does not contain MRI Safety Information
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
FPA Set, administration, intravascular

GMDN Terms

Code Name
35833 Electric infusion pump administration set, single-use

Identifiers

Type ID
Package 05705244027183
Primary 05705244027206
Package 05705244027190

Customer Contacts

Phone
+18004228811

Device Sizes

Type Value Unit Text
Angle 90 degree
Length 80 Centimeter
Depth 9 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a cool, dry location at room temperature. Do not store in direct sunlight, or in high humidity.