FDA UDI In Commercial Distribution 🇺🇸 United States

PERLA ® TL

DI: 07640185346642 · Model: TLF-5P T0 40-S · SpineArt SA
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PERLA ® TL
Primary DI
07640185346642
Version / Model
TLF-5P T0 40-S
Catalog Number
TLF-5P T0 40-S
Company Name
SpineArt SA
Labeler DUNS
483016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-02-11
Public Version
2
Public Version Date
2020-04-10
Public Version Status
Update
Public Device Record Key
dc7ef67e-cc95-4203-bf87-ad5fa1db08a5

Device Description

PREBENT ROD TITANIUM Ø5.5 L40

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
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 07640185346642

Device Sizes

Type Value Unit Text
Outer Diameter 5.5 Millimeter
Length 40 Millimeter