FDA UDI In Commercial Distribution 🇺🇸 United States

PERLA ® TL

DI: 07640332470299 · Model: TLF-6Z T4 50-S · SpineArt SA
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PERLA ® TL
Primary DI
07640332470299
Version / Model
TLF-6Z T4 50-S
Catalog Number
TLF-6Z T4 50-S
Company Name
SpineArt SA
Labeler DUNS
483016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-11-03
Public Version
1
Public Version Date
2023-11-13
Public Version Status
New
Public Device Record Key
f014a5a3-ae85-41ef-ad4d-53458f7ef5bf

Device Description

KIT OF 2 Z RODS Ø6 TITANIUM L150+300 Ø6 L450

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
MR Conditional
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
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KWP Appliance, Fixation, Spinal Interlaminal
NKB Thoracolumbosacral Pedicle Screw System

GMDN Terms

Code Name
61324 Bone-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary 07640332470299

Device Sizes

Type Value Unit Text
Length 450 Millimeter
Outer Diameter 6 Millimeter