FDA UDI In Commercial Distribution 🇺🇸 United States

neria™soft

DI: 05705244000339 · Model: 79-030-2522 · Unomedical A/S
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
neria™soft
Primary DI
05705244000339
Version / Model
79-030-2522
Company Name
Unomedical A/S
Labeler DUNS
306032491
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-09-15
Public Version
3
Public Version Date
2020-03-12
Public Version Status
Update
Public Device Record Key
9f17c4ed-414a-4a57-b6af-1a2c8f728896

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
Primary 05705244000339
Unit of Use 05705244011007
Package 05705244000346

Device Sizes

Type Value Unit Text
Length 30 Centimeter
Depth 13 Millimeter
Angle 30 degree

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Protect from direct sunlight. Store at room temperature.