LES ENCRES DVSOR19100W-00170X

GUDID 08800256050062

MEDITIME CO., LTD.

Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial Polyester suture, bioabsorbable, monofilament, non-antimicrobial

Primary Device ID	08800256050062
NIH Device Record Key	a17210c0-49fa-4789-82d5-fb033845902f
Commercial Distribution Status	In Commercial Distribution
Brand Name	LES ENCRES
Version Model Number	DVSOR19100W-00170X
Catalog Number	DVSOR19100W-00170X
Company DUNS	689774482
Company Name	MEDITIME CO., LTD.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800256050062 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K190264

FDA Product Code

NEW	Suture, Surgical, Absorbable, Polydioxanone

Sterilization

Steralize Prior To Use	false
Device Is Sterile	true

Device Entry Metadata

Public Version Status	New
Device Record Status	Published
Public Version Number	1
Public Version Date	2024-05-10
Device Publish Date	2024-05-02

On-Brand Devices [LES ENCRES]

08800256050260	DVAGP19120W-00170E
08800256050253	DVAGP19100W-00160E
08800256050208	DVCHR19038L-00040X
08800256050116	DVSRR21100W-30150X
08800256050109	DVSRR19100W-00170X
08800256050093	DVSOR21100L-30150X
08800256050086	DVSOR21060L-30130X
08800256050079	DVSOR19120W-00200X
08800256050062	DVSOR19100W-00170X
08800256050055	DVSOP19120W-00180E
08800256050048	DVSOP19100W-00160E

Trademark Results [LES ENCRES]

Mark Image Registration \| Serial	Company Trademark Application Date
LES ENCRES 88364614 5895210 Live/Registered	Reynolds, Stacey 2019-03-31