AutoSoft 90

GUDID 05705244018310

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 ID05705244018310
NIH Device Record Keyadb44c07-2268-46a9-ab50-2dfcf489cedc
Commercial Distribution StatusIn Commercial Distribution
Brand NameAutoSoft 90
Version Model Number1002823
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

Customer Support Contacts

Phone1-858-255-6269
Emailxx@xx.xx

Device Dimensions

Angle90 degree
Angle90 degree
Angle90 degree

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Protect from direct sunlight and atmospheric humidity. Store in a dry place at room temperature.

Device Identifiers

Device Issuing AgencyDevice ID
GS105705244018303 [Primary]
GS105705244018310 [Package]
Contains: 05705244018303
Package: Outer Box [100 Units]
In Commercial Distribution
GS105705244018327 [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 Number2
Public Version Date2020-03-30
Device Publish Date2019-03-15

On-Brand Devices [AutoSoft 90]

05705244018341Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244018310Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244018280Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244018259Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244018228Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244018198Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244018167Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244018136Single use infusion set for subcutaneous infusion. The infusion set must be used as described in
05705244014572Single use infusion set for subcutaneous infusion. The infusion set must be used as described
05705244014558Single use infusion set for subcutaneous infusion. The infusion set must be used as described
05705244014527Single use infusion set for subcutaneous infusion. The infusion set must be used as described
05705244014992Single use infusion set for subcutaneous infusion. The infusion set must be used as described
05705244014466Single use infusion set for subcutaneous infusion. The infusion set must be used as described
05705244014435Single use infusion set for subcutaneous infusion. The infusion set must be used as described
05705244014404Single use infusion set for subcutaneous infusion. The infusion set must be used as described
05705244014374Single use infusion set for subcutaneous infusion. The infusion set must be used as described
05705244014343Single use infusion set for subcutaneous infusion. The infusion set must be used as described
05705244014312Single use infusion set for subcutaneous infusion. The infusion set must be used as described

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