FDA UDI In Commercial Distribution 🇺🇸 United States

IntraLock

DI: 00840124507500 · Model: TN-LL-5861 · FUSION ORTHOPEDICS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
IntraLock
Primary DI
00840124507500
Version / Model
TN-LL-5861
Catalog Number
TN-LL-5861
Company Name
FUSION ORTHOPEDICS, LLC
Labeler DUNS
080307067
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-05-12
Public Version
2
Public Version Date
2023-06-14
Public Version Status
Update
Public Device Record Key
e2ff273a-6ef7-4309-8300-872d5bbc35af

Device Description

LapiLock Reese Guide 6mm

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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
Yes

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
60826 Custom-made orthopaedic/craniofacial surgical guide

Identifiers

Type ID
Primary 00840124507500