STEEL WIRE

GUDID E203USL99068

Resorba Medical GmbH

Metallic suture, monofilament
Primary Device IDE203USL99068
NIH Device Record Key6048a6d7-0425-441f-b3c3-83ec2c49b1a5
Commercial Distribution StatusIn Commercial Distribution
Brand NameSTEEL WIRE
Version Model NumberSTEEL WIRE
Company DUNS341053195
Company NameResorba Medical GmbH
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 Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCE203USL99068 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GAQSuture, Nonabsorbable, Steel, Monofilament And Multifilament, Sterile

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-05-07
Device Publish Date2019-01-21

On-Brand Devices [STEEL WIRE]

E203USL99071STEEL WIRE
E203USL99070STEEL WIRE
E203USL99069STEEL WIRE
E203USL99068STEEL WIRE
E203USL99067STEEL WIRE
E203USL99066STEEL WIRE
E203USL99065STEEL WIRE
E203USL99064STEEL WIRE
E203USL99063STEEL WIRE
E203USL99061STEEL WIRE

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