FDA UDI In Commercial Distribution 🇺🇸 United States

LACTOSORB® SCREW SYSTEM

DI: 00880304416277 · Model: 950049 · Biomet Orthopedics, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LACTOSORB® SCREW SYSTEM
Primary DI
00880304416277
Version / Model
950049
Catalog Number
950049
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-06-11
Public Version
1
Public Version Date
2019-06-19
Public Version Status
New
Public Device Record Key
33e5e30c-c5a2-4d0c-bbfb-1cc4b571a29d

Device Characteristics

Single Use
No
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HWR DRIVER, PROSTHESIS

GMDN Terms

Code Name
32865 Orthopaedic implant driver

Identifiers

Type ID
Primary 00880304416277

Customer Contacts