FDA UDI In Commercial Distribution 🇺🇸 United States

IntraLock LapiLock

DI: 00840124506930 · Model: TN-LL-0001 · FUSION ORTHOPEDICS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
IntraLock LapiLock
Primary DI
00840124506930
Version / Model
TN-LL-0001
Catalog Number
TN-LL-0001
Company Name
FUSION ORTHOPEDICS, LLC
Labeler DUNS
080307067
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-10
Public Version
2
Public Version Date
2023-06-14
Public Version Status
Update
Public Device Record Key
51a08327-8bee-4c63-a577-234d0c2c0c39

Device Description

LapiLock Hohmann Retractor Short

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
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
HWC Screw, Fixation, Bone

GMDN Terms

Code Name
42500 Dressing/utility forceps, tweezers-like, reusable

Identifiers

Type ID
Primary 00840124506930