FDA UDI In Commercial Distribution 🇺🇸 United States

CONELOG® X-Ray Planning foil

DI: E219C530090101 · Model: C5300.9010 · ALTATEC GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CONELOG® X-Ray Planning foil
Primary DI
E219C530090101
Version / Model
C5300.9010
Catalog Number
C5300.9010
Company Name
ALTATEC GmbH
Labeler DUNS
322018193
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-08
Public Version
1
Public Version Date
2022-12-16
Public Version Status
New
Public Device Record Key
c9c8bdaa-e385-425d-aa3f-e9372dae1a78

Device Description

CONELOG® X-Ray Planning foil 1:1.25 for CONELOG® SCREW-LINE implants, Magnification 25%

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
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NDP Accessories, Implant, Dental, Endosseous

GMDN Terms

Code Name
47974 Dental implant x-ray template

Identifiers

Type ID
Primary E219C530090101

Customer Contacts

Phone
7609181857