PDO M303

GUDID 10790986006383

C.P. MEDICAL CORPORATION

Polyester suture, bioabsorbable, monofilament, non-antimicrobial
Primary Device ID10790986006383
NIH Device Record Key93ae6cbd-6c96-4940-b97a-7abde6255d2e
Commercial Distribution StatusIn Commercial Distribution
Brand NamePDO
Version Model NumberM303
Catalog NumberM303
Company DUNS807404611
Company NameC.P. MEDICAL CORPORATION
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 Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS110790986006383 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NEWSuture, Surgical, Absorbable, Polydioxanone

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[10790986006383]

Ethylene Oxide


[10790986006383]

Ethylene Oxide


[10790986006383]

Ethylene Oxide


[10790986006383]

Ethylene Oxide


[10790986006383]

Ethylene Oxide


[10790986006383]

Ethylene Oxide


[10790986006383]

Ethylene Oxide


[10790986006383]

Ethylene Oxide


[10790986006383]

Ethylene Oxide


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number6
Public Version Date2021-02-05
Device Publish Date2016-02-23

On-Brand Devices [PDO]

10790986006390M463
10790986006383M303

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