FDA UDI In Commercial Distribution 🇺🇸 United States

JULIET TL

DI: 07640375234780 · Model: DYN-IT 01 05-N · SpineArt SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
JULIET TL
Primary DI
07640375234780
Version / Model
DYN-IT 01 05-N
Catalog Number
DYN-IT 01 05-N
Company Name
SpineArt SA
Labeler DUNS
483016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-11-10
Public Version
1
Public Version Date
2025-11-18
Public Version Status
New
Public Device Record Key
9a18ae29-57f4-444c-b5c5-125ee57bd687

Device Description

ANTI-ROTATION IMPLANT HOLDER TUBE

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
No
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
47807 Surgical implant/trial-implant/sizer holder, reusable

Identifiers

Type ID
Primary 07640375234780