FDA UDI In Commercial Distribution 🇺🇸 United States

Direct Inject

DI: 07613327123272 · Model: 79-45910 · Stryker Leibinger GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Direct Inject
Primary DI
07613327123272
Version / Model
79-45910
Catalog Number
79-45910
Company Name
Stryker Leibinger GmbH & Co. KG
Labeler DUNS
316153956
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
4
Public Version Date
2020-06-19
Public Version Status
Update
Public Device Record Key
37319a40-7b0b-41bc-9010-f4ba44cbcdf0

Device Description

DirectInject On-Demand HA Cement

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GXP METHYL METHACRYLATE FOR CRANIOPLASTY

GMDN Terms

Code Name
17751 Bone matrix implant, synthetic, non-antimicrobial

Identifiers

Type ID
Primary 07613327123272

Premarket Submissions

Submission Number Supplement Number
K143661 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Total Volume: 10.0 Cubic Centimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
59 – 77 Degrees Fahrenheit