FDA UDI In Commercial Distribution 🇺🇸 United States

ARCADIUS® XP C

DI: 04046964942549 · Model: ME103 · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
ARCADIUS® XP C
Primary DI
04046964942549
Version / Model
ME103
Catalog Number
ME103
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2019-03-01
Public Version
4
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
4a55b7be-a803-4fad-bf49-074e55f83593

Device Description

ARCADIUS XP C U-JOINT SOFT TISSUE PROT.

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
OVE Intervertebral fusion device with integrated fixation, cervical

GMDN Terms

Code Name
58927 Orthopaedic prosthesis implantation positioning instrument, single-use

Identifiers

Type ID
Primary 04046964942549
Unit of Use 04046964942532

Customer Contacts