Viamed Surgical Blades

GUDID 36945630112400

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
Primary Device ID36945630112400
NIH Device Record Keye01b012f-acb5-460b-9404-1820b31248ce
Commercial Distribution StatusIn Commercial Distribution
Brand NameViamed Surgical Blades
Version Model Number12#
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
GS106945630112409 [Unit of Use]
GS116945630112406 [Primary]
GS136945630112400 [Package]
Contains: 16945630112406
Package: [5000 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 Date2022-05-26
Device Publish Date2022-05-18

On-Brand Devices [Viamed Surgical Blades]

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

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