FDA UDI In Commercial Distribution 🇺🇸 United States

RAPHAEL

DI: 00841732123779 · Model: 015.3962 · CTL MEDICAL CORPORATION
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RAPHAEL
Primary DI
00841732123779
Version / Model
015.3962
Company Name
CTL MEDICAL CORPORATION
Labeler DUNS
080138504
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-07
Public Version
1
Public Version Date
2023-09-15
Public Version Status
New
Public Device Record Key
8ca25306-c145-4375-be1f-57b7ffd389c6

Device Description

RAPHAEL™ Polyaxial Reduction Screw, LX, 5.5 x L60mm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
KWP Appliance, Fixation, Spinal Interlaminal
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 00841732123779

Premarket Submissions

Submission Number Supplement Number
K132365 000