FDA UDI In Commercial Distribution 🇺🇸 United States

HYDROSET

DI: 07613154275021 · Model: 79-43915 · Stryker Leibinger GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HYDROSET
Primary DI
07613154275021
Version / Model
79-43915
Catalog Number
79-43915
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
3
Public Version Date
2020-06-19
Public Version Status
Update
Public Device Record Key
4f88305b-2107-444d-b9f3-6fdd3c62cd55

Device Description

15CC HYDROSET INJECTABLE 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
No
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 07613154275021

Device Sizes

Type Value Unit Text
Device Size Text, specify Total Volume: 15.0 Cubic Centimeter