FDA UDI In Commercial Distribution 🇺🇸 United States

Vanguard® Slidex® Knee Instrument

DI: 00887868493904 · Model: 32-485109 · Biomet Orthopedics, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
2

Basic Information

Brand Name
Vanguard® Slidex® Knee Instrument
Primary DI
00887868493904
Version / Model
32-485109
Catalog Number
32-485109
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2022-07-07
Public Version
1
Public Version Date
2022-07-15
Public Version Status
New
Public Device Record Key
3c9e42b0-e6e0-4f57-8d6e-d590487f18cf

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
No
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
FZX Guide, surgical, instrument

GMDN Terms

Code Name
47829 Surgical instrument handle, non-torque-limiting

Identifiers

Type ID
Unit of Use 70887868493903
Primary 00887868493904

Customer Contacts