naturesQue MaxOss P

GUDID 00813954023434

Anorganic Bone Mineral

COLLAGEN MATRIX, INC.

Dental bone matrix implant, animal-derived
Primary Device ID00813954023434
NIH Device Record Key76667f5a-0c3c-4379-b0a5-4b09d154dc96
Commercial Distribution StatusIn Commercial Distribution
Brand NamenaturesQue MaxOss P
Version Model Number58489
Company DUNS176262442
Company NameCOLLAGEN MATRIX, 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 Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100813954023434 [Primary]

FDA Product Code

NPMBone Grafting Material, Animal Source

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-03-04
Device Publish Date2020-02-25

On-Brand Devices [naturesQue MaxOss P]

00813954023496Anorganic Bone Mineral in Syringe
00813954023489Anorganic Bone Mineral in Syringe
00813954023472Anorganic Bone Mineral
00813954023465Anorganic Bone Mineral
00813954023458Anorganic Bone Mineral
00813954023441Anorganic Bone Mineral
00813954023434Anorganic Bone Mineral
00813954023427Anorganic Bone Mineral

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