FDA UDI In Commercial Distribution 🇺🇸 United States

JULIET Ti PO

DI: 07640332471012 · Model: JUL-BX 40 11-N · SpineArt SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
JULIET Ti PO
Primary DI
07640332471012
Version / Model
JUL-BX 40 11-N
Catalog Number
JUL-BX 40 11-N
Company Name
SpineArt SA
Labeler DUNS
483016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-11-20
Public Version
1
Public Version Date
2025-11-28
Public Version Status
New
Public Device Record Key
8ffcd0cb-600a-4fe3-954a-c93fdcaa2362

Device Description

JULIET COMBO SET - TRIALS RACK PO NARROW

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
FSM Tray, Surgical, Instrument

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Primary 07640332471012