FDA UDI In Commercial Distribution 🇺🇸 United States

icotec Cervical Cage, Cervical Cage Anatomic, Container, complete

DI: 07640140433783 · Model: 41-12 · icotec AG
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
icotec Cervical Cage, Cervical Cage Anatomic, Container, complete
Primary DI
07640140433783
Version / Model
41-12
Catalog Number
41-12
Company Name
icotec AG
Labeler DUNS
480789465
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-07-16
Public Version
7
Public Version Date
2023-09-11
Public Version Status
Update
Public Device Record Key
c3ebd595-62af-4f84-bb78-ac994b5dda82

Device Description

icotec Cervical Cage, Cervical Cage Anatomic, Container, complete

Device Characteristics

Single Use
No
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ODP Intervertebral Fusion Device With Bone Graft, Cervical

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Primary 07640140433783

Customer Contacts

Phone
+41717570000