FDA UDI In Commercial Distribution 🇺🇸 United States

SKYLINE

DI: 10705034412016 · Model: 186802040S · Medos International Sàrl
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SKYLINE
Primary DI
10705034412016
Version / Model
186802040S
Catalog Number
186802040S
Company Name
Medos International Sàrl
Labeler DUNS
482661753
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-05
Public Version
2
Public Version Date
2023-01-11
Public Version Status
Update
Public Device Record Key
f42ad1dc-8b7a-48a2-b3e8-51bb9a09d3f1

Device Description

SKYLINE ANTERIOR CERVICAL PLATE SYSTEM TWO LEVEL PLATE 40mm

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KWQ Appliance, fixation, spinal intervertebral body

GMDN Terms

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

Identifiers

Type ID
Primary 10705034412016

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K132324 000
K171439 000