MOPYLEN

GUDID E203US71510

Resorba Medical GmbH

Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament Polyolefin/fluoropolymer suture, monofilament
Primary Device IDE203US71510
NIH Device Record Key2eb77c60-bbcf-42f3-b047-32ece02fa556
Commercial Distribution StatusIn Commercial Distribution
Brand NameMOPYLEN
Version Model NumberMOPYLEN
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
HIBCCE203US71510 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GAWSuture, Nonabsorbable, Synthetic, Polypropylene

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-04-08
Device Publish Date2019-01-24

On-Brand Devices [MOPYLEN]

E203US7173MOPYLEN
E203US7157MOPYLEN
E203US7156MOPYLEN
E203US7155MOPYLEN
E203US71530MOPYLEN
E203US71526MOPYLEN
E203US71521MOPYLEN
E203US7152MOPYLEN
E203US71514MOPYLEN
E203US71513MOPYLEN
E203US71512MOPYLEN
E203US71511MOPYLEN
E203US71510MOPYLEN
E203US7149MOPYLEN
E203US7148MOPYLEN
E203US71418MOPYLEN
E203US71415MOPYLEN
E203US7076MOPYLEN
E203US70737MOPYLEN
E203US70718MOPYLEN
E203US70711MOPYLEN
E203US7038MOPYLEN
E203US7035MOPYLEN
E203US7034MOPYLEN
E203US7033MOPYLEN
E203US7032MOPYLEN
E203US7031MOPYLEN
E203US7026MOPYLEN
E203US7025MOPYLEN
E203US70244MOPYLEN
E203US70243MOPYLEN
E203US70241MOPYLEN
E203US70240MOPYLEN
E203US70238MOPYLEN
E203US70222MOPYLEN
E203US70221MOPYLEN
E203US70220MOPYLEN
E203US70219MOPYLEN
E203US70218MOPYLEN
E203US70217MOPYLEN
E203US70215MOPYLEN
E203US70212MOPYLEN
E203US70211MOPYLEN
E203US70210MOPYLEN
E203US7077MOPYLEN
E203US7094MOPYLEN
E203US70712MOPYLEN
E203US71550MOPYLEN
E203US71436MOPYLEN

Trademark Results [MOPYLEN]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MOPYLEN
MOPYLEN
79182321 5024689 Live/Registered
Resorba Medical GmbH
2016-01-13

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