neria™ detach

GUDID 05705244000957

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

Unomedical A/S

Electric infusion pump administration set, single-use

Primary Device ID	05705244000957
NIH Device Record Key	dc3631f7-3e48-4272-9610-400fa8cad2ed
Commercial Distribution Status	In Commercial Distribution
Brand Name	neria™ detach
Version Model Number	78-110-2726
Company DUNS	306032491
Company Name	Unomedical A/S
Device Count	10
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Dimensions

Length	110 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	110 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	110 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	110 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	110 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	110 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	110 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	110 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	110 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	110 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	110 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	110 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	110 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	110 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	110 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	110 Centimeter
Depth	6 Millimeter
Angle	90 degree
Length	110 Centimeter
Depth	6 Millimeter
Angle	90 degree

Operating and Storage Conditions

Special Storage Condition, Specify	Between 0 and 0 *Protect from direct sunlight. Store at room temperature
Special Storage Condition, Specify	Between 0 and 0 *Protect from direct sunlight. Store at room temperature
Special Storage Condition, Specify	Between 0 and 0 *Protect from direct sunlight. Store at room temperature
Special Storage Condition, Specify	Between 0 and 0 *Protect from direct sunlight. Store at room temperature
Special Storage Condition, Specify	Between 0 and 0 *Protect from direct sunlight. Store at room temperature
Special Storage Condition, Specify	Between 0 and 0 *Protect from direct sunlight. Store at room temperature
Special Storage Condition, Specify	Between 0 and 0 *Protect from direct sunlight. Store at room temperature
Special Storage Condition, Specify	Between 0 and 0 *Protect from direct sunlight. Store at room temperature
Special Storage Condition, Specify	Between 0 and 0 *Protect from direct sunlight. Store at room temperature
Special Storage Condition, Specify	Between 0 and 0 *Protect from direct sunlight. Store at room temperature
Special Storage Condition, Specify	Between 0 and 0 *Protect from direct sunlight. Store at room temperature
Special Storage Condition, Specify	Between 0 and 0 *Protect from direct sunlight. Store at room temperature
Special Storage Condition, Specify	Between 0 and 0 *Protect from direct sunlight. Store at room temperature
Special Storage Condition, Specify	Between 0 and 0 *Protect from direct sunlight. Store at room temperature
Special Storage Condition, Specify	Between 0 and 0 *Protect from direct sunlight. Store at room temperature
Special Storage Condition, Specify	Between 0 and 0 *Protect from direct sunlight. Store at room temperature
Special Storage Condition, Specify	Between 0 and 0 *Protect from direct sunlight. Store at room temperature

Device Identifiers

Device Issuing Agency	Device ID
GS1	05705244000957 [Primary]
GS1	05705244000964 [Package] Package: Outer box [200 Units] In Commercial Distribution
GS1	05705244010895 [Unit of Use]

FDA Product Code

FPA	Set, Administration, Intravascular

Sterilization

Steralize Prior To Use	false
Device Is Sterile	true

Device Entry Metadata

Public Version Status	Update
Device Record Status	Published
Public Version Number	2
Public Version Date	2018-03-29
Device Publish Date	2016-09-15

On-Brand Devices [neria™ detach]

05705244000995	Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244000971	Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244000957	Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244000933	Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244000919	Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244000896	Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244000872	Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244000858	Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244000834	Single use infusion set for subcutaneous infusion. The infusion set must be used as described in

Trademark Results [neria]

Mark Image Registration \| Serial	Company Trademark Application Date
NERIA 79063901 3771683 Live/Registered	Unomedical A/S 2008-11-28