FDA UDI Not in Commercial Distribution 🇺🇸 United States

PERLA ®

DI: 07640151097196 · Model: CPF-PR T0 65-S · SpineArt SA
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PERLA ®
Primary DI
07640151097196
Version / Model
CPF-PR T0 65-S
Catalog Number
CPF-PR T0 65-S
Company Name
SpineArt SA
Labeler DUNS
483016148
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-07-11
Public Version
3
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
812e97be-a292-4ea1-a777-9f02ed5c5eb0
Distribution End Date
2019-02-06

Device Description

PREBENT ROD TITANIUM

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
NKG Orthosis, Cervical Pedicle Screw Spinal Fixation

GMDN Terms

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

Identifiers

Type ID
Package 07640151100247
Primary 07640151097196

Device Sizes

Type Value Unit Text
Outer Diameter 3.5 Millimeter
Length 65 Millimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius