TRUSILK

GUDID 08903837048677

HEALTHIUM MEDTECH LIMITED

Silk suture
Primary Device ID08903837048677
NIH Device Record Key1f5fe6d8-f7f4-4254-a484-74196f5a7cd4
Commercial Distribution StatusIn Commercial Distribution
Brand NameTRUSILK
Version Model Number5F75DZ26
Company DUNS916326705
Company NameHEALTHIUM MEDTECH LIMITED
Device Count1
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 Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108903837048677 [Primary]

FDA Product Code

GAPSuture, Nonabsorbable, Silk

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-02-24
Device Publish Date2025-02-15

On-Brand Devices [TRUSILK]

089038370393855F45CX26
089038372294345G45CX16
089038372294105F45CX30
089038372293735F45CX20
089038370486775F75DZ26
089038370473285E75DZ26
089038370462605D75DZ26

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.