VIAMED SURGICAL BLADES

GUDID 36945630121662

Sterilance Medical (Suzhou) Inc.

Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use Manual scalpel blade, single-use
Primary Device ID36945630121662
NIH Device Record Keya63592c4-c260-49e0-aad5-1a14a4c1cc0c
Commercial Distribution StatusIn Commercial Distribution
Brand NameVIAMED SURGICAL BLADES
Version Model Number15C
Company DUNS554434897
Company NameSterilance Medical (Suzhou) Inc.
Device Count100
DM Exemptfalse
Pre-market Exempttrue
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 Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS106945630121661 [Unit of Use]
GS116945630121668 [Primary]
GS136945630121662 [Package]
Contains: 16945630121668
Package: [50 Units]
In Commercial Distribution

FDA Product Code

GESBlade, Scalpel

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-11-08
Device Publish Date2023-10-31

On-Brand Devices [VIAMED SURGICAL BLADES]

3694563011246224#
3694563011245523#
3694563011244822#
3694563011243121#
3694563011242420#
3694563011241715#
3694563011240012#
3694563011239411#
3694563011238710#
3694563012166215C

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