FDA UDI In Commercial Distribution 🇺🇸 United States

CONELOG® Re-Set™ cam ring remover

DI: E219C591050001 · Model: C5910.5000 · ALTATEC GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CONELOG® Re-Set™ cam ring remover
Primary DI
E219C591050001
Version / Model
C5910.5000
Catalog Number
C5910.5000
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
fd95f1a1-86f7-43e7-b47f-f821618b7e3f

Device Description

CONELOG® Re-Set™ cam ring remover for d 5.0 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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NDP Accessories, Implant, Dental, Endosseous

GMDN Terms

Code Name
45319 Dental implant extractor

Identifiers

Type ID
Primary E219C591050001

Customer Contacts

Phone
7609181857