FDA UDI In Commercial Distribution 🇺🇸 United States

ARCADIUS® XP L

DI: 04046964861000 · Model: ME178T · AESCULAP IMPLANT SYSTEMS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ARCADIUS® XP L
Primary DI
04046964861000
Version / Model
ME178T
Catalog Number
ME178T
Company Name
AESCULAP IMPLANT SYSTEMS, LLC
Labeler DUNS
622600992
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-31
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
b049bc7c-e7fe-4a4a-a063-af018ebb4a51

Device Description

ARCADIUS COMPRESSION BONE SCREW 30 MM

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
No
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
OVD Intervertebral fusion device with integrated fixation, lumbar

GMDN Terms

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

Identifiers

Type ID
Primary 04046964861000

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Length : 30.000 MM
Device Size Text, specify Diameter (mm) : 4.500 MM