PuraPly Micronized Wound Matrix (PuraPly MZ)

GUDID 00618474000404

PuraPly® Micronized Wound Matrix (PuraPly® MZ) consists of micronized porcine collagen intended for the management of wounds. PuraPly® Micronized Wound Matrix is supplied as a dry powder of particle size of less than or equal to 1000. The device is sterile and packaged in a vial sealed in a single pouch.

ORGANOGENESIS INC.

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Primary Device ID00618474000404
NIH Device Record Keyd4fc2c34-e25c-4d7d-8c80-cd15ef684cd5
Commercial Distribution StatusIn Commercial Distribution
Brand NamePuraPly Micronized Wound Matrix (PuraPly MZ)
Version Model Number515-061
Company DUNS152165817
Company NameORGANOGENESIS 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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Weight500 Milligram
Weight500 Milligram
Weight500 Milligram
Weight500 Milligram
Weight500 Milligram
Weight500 Milligram
Weight500 Milligram
Weight500 Milligram
Weight500 Milligram
Weight500 Milligram
Weight500 Milligram
Weight500 Milligram
Weight500 Milligram
Weight500 Milligram
Weight500 Milligram
Weight500 Milligram
Weight500 Milligram

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Do not freeze or expose to excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Do not freeze or expose to excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Do not freeze or expose to excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Do not freeze or expose to excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Do not freeze or expose to excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Do not freeze or expose to excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Do not freeze or expose to excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Do not freeze or expose to excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Do not freeze or expose to excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Do not freeze or expose to excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Do not freeze or expose to excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Do not freeze or expose to excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Do not freeze or expose to excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Do not freeze or expose to excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Do not freeze or expose to excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Do not freeze or expose to excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Do not freeze or expose to excess heat

Device Identifiers

Device Issuing AgencyDevice ID
GS100618474000404 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KGNWound Dressing With Animal-Derived Material(S)

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-05-09
Device Publish Date2023-05-01

On-Brand Devices [PuraPly Micronized Wound Matrix (PuraPly MZ) ]

00618474000411PuraPly® Micronized Wound Matrix (PuraPly® MZ) consists of micronized porcine collagen intende
00618474000404PuraPly® Micronized Wound Matrix (PuraPly® MZ) consists of micronized porcine collagen intende
00618474000398PuraPly® Micronized Wound Matrix (PuraPly® MZ) consists of micronized porcine collagen intende

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