FDA UDI In Commercial Distribution 🇺🇸 United States

Autosoft™ XC

DI: 05705244026049 · Model: 1009566 · Unomedical A/S
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
2

Basic Information

Brand Name
Autosoft™ XC
Primary DI
05705244026049
Version / Model
1009566
Catalog Number
N/A
Company Name
Unomedical A/S
Labeler DUNS
306032491
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2023-06-13
Public Version
1
Public Version Date
2023-06-21
Public Version Status
New
Public Device Record Key
19a9f771-12e6-435a-b3df-2f152b5ec0ef

Device Description

Single use infusion set for subcutaneous infusion. The infusion set must be used as described in the Instruction for Use.

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 05705244026056
Primary 05705244026049
Unit of Use 05705244026063

Customer Contacts

Phone
9999999999

Device Sizes

Type Value Unit Text
Angle 90 degree
Depth 6 Millimeter
Length 12 Centimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store infusion sets in a cool, dry location at room temperature 15 to 25 C. Do not store infusion sets in direct sunlight, or in high humidity.