neria™soft 90

GUDID 05705244003675

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 ID05705244003675
NIH Device Record Keybbe5daef-8a5e-4fe1-a151-04cbbf83fc09
Commercial Distribution StatusIn Commercial Distribution
Brand Nameneria™soft 90
Version Model Number722060-5226
Company DUNS306032491
Company NameUnomedical A/S
Device Count10
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Angle90 degree
Angle90 degree
Angle90 degree

Operating and Storage Conditions

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

Device Identifiers

Device Issuing AgencyDevice ID
GS105705244003675 [Primary]
GS105705244003682 [Package]
Package: Outer box [100 Units]
In Commercial Distribution
GS105705244010376 [Unit of Use]

FDA Product Code

FPASet, Administration, Intravascular

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2020-03-18
Device Publish Date2016-09-15

On-Brand Devices [neria™soft 90]

05705244003996Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244003972Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244003736Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244003712Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244003699Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244003675Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244003651Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244003637Single 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
NERIA
79063901 3771683 Live/Registered
Unomedical A/S
2008-11-28

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.