FDA UDI In Commercial Distribution 🇺🇸 United States

FANELLI GUIDE

DI: 00880304412552 · Model: 909800 · Biomet Orthopedics, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FANELLI GUIDE
Primary DI
00880304412552
Version / Model
909800
Catalog Number
909800
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-07-28
Public Version
3
Public Version Date
2018-11-22
Public Version Status
Update
Public Device Record Key
c620f27d-6f2a-4a93-8d12-68a9c72c5d38

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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
47786 Orthopaedic implant aiming arm

Identifiers

Type ID
Primary 00880304412552

Customer Contacts