Mobius Elastic Retractor

GUDID 20888937003783

Small; 4-9 cm Incision Range

Coopersurgical, Inc.

Self-retaining surgical retractor, single-use
Primary Device ID20888937003783
NIH Device Record Key59249d89-2309-4183-a10f-b9717a3fe105
Commercial Distribution StatusIn Commercial Distribution
Brand NameMobius Elastic Retractor
Version Model Number900-500
Company DUNS801895244
Company NameCoopersurgical, Inc.
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100888937003789 [Primary]
GS120888937003783 [Package]
Contains: 00888937003789
Package: [5 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GCJLaparoscope, General & Plastic Surgery

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-06-07

On-Brand Devices [Mobius Elastic Retractor]

20888937003820Large; 12-17 cm Incision Range
20888937003813Medium-Large; 10-15 cm Incision Range
20888937003806Medium; 8-14 cm Incision Range
20888937003790Mini; 2-6 cm Incision Range
20888937003783Small; 4-9 cm Incision Range

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