VertaPlex

Primary DI
07613252254430
Brand
VertaPlex
Company
STRYKER CORPORATION
Model
0406622000
Catalog number
0406-622-000
Device description
High Viscosity Radiopaque Bone Cement
Published
2016-09-23
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Safe
Rx
true
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
LODBONE CEMENT
NDNCEMENT, BONE, VERTEBROPLASTY
PMLbone cement, posterior screw augmentation

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LODBone CementOrthopedic2
NDNCement, Bone, VertebroplastyOrthopedic2
PMLBone Cement, Posterior Screw AugmentationOrthopedic2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
37613252254431PackageGS12In Commercial Distribution
07613252254430PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
3761325225443137613252254431
07613252254430076132522544307613252254430

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic bone void filling material, synthetic, non-bioabsorbableA non-bioabsorbable, implantable device made of a synthetic material(s) intended to replace bone lost through trauma, surgery, or pathological conditions (e.g., osteoporosis); it is not dedicated to dental applications and is not intended for implant fixation (not a bone cement). It may be a powder [e.g., polymethylmethacrylate (PMMA)], or a non-PMMA-containing elastomer formed by mixing two precursors, prior to implantation typically during a balloon kyphoplasty or vertebroplasty procedure; it does not include an antimicrobial agent(s). It may also be referred to as a bone augmentation material.

Contacts#

Phone, Email table
PhoneEmail
+0118002533210INST.STRYKER.CS@STRYKER.COM

Regulatory Flags#

DUNS number
196548481
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
07613327665031Sonopet iQ+550026B0105500-26B-0102026-10-12
07613327665048Sonopet iQ+550026B0205500-26B-0202026-10-12
07613327665055Sonopet iQ+550026B1145500-26B-1142026-10-12
07613327665062Sonopet iQ+550026B3125500-26B-3122026-10-12
07613327687149Sonopet iQ+550026B3285500-26B-3282026-10-12
07613327662030ALPHAVENT3911-856-5473911-856-5472025-06-16
07613327662047ALPHAVENT3911-856-5553911-856-5552025-06-16
07613327662054ALPHAVENT3911-856-5653911-856-5652025-06-16
04546540434364SpinePlex04062020000406-202-0002016-06-30
07613327141788SpinePlex04062020100406-202-0102016-09-23
07613154757091VertaPlex04064020000406-402-0002016-06-30
07613327141764VertaPlex04064020020406-402-0022016-09-23
07613327170559VertaPlex HV04066220150406-622-0152016-09-23
07613327170566VertaPlex04064020150406-402-0152016-09-23
00808232000214NA2102-01312102-01312015-09-24
07613327124200Vitoss VBA Pack2102-24012102-24012015-12-09
07613327124217Vitoss VBA Pack2101-24052102-24052015-12-09
07613327124224Vitoss VBA Pack2102-24022102-24022015-12-09
07613327124231Vitoss VBA Pack2102-24102102-24102015-12-09
07613327176940NA3102-10023102-10022015-10-24

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