Max V Radiopaque Cement 10001158

GUDID 03760177047419

TEKNIMED

Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable Vertebral bone filler, non-bioabsorbable
Primary Device ID03760177047419
NIH Device Record Keya96f7fdc-9446-412f-9add-a22674cb3efd
Commercial Distribution StatusIn Commercial Distribution
Brand NameMax V Radiopaque Cement
Version Model NumberNuVasive Maximum Viscosity Cement
Catalog Number10001158
Company DUNS764746723
Company NameTEKNIMED
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

Operating and Storage Conditions

Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius
Storage Environment TemperatureBetween 0 Degrees Celsius and 25 Degrees Celsius

Device Identifiers

Device Issuing AgencyDevice ID
GS103760177047419 [Primary]

FDA Product Code

NDNCement, Bone, Vertebroplasty

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-12-01
Device Publish Date2020-11-23

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