FDA UDI In Commercial Distribution 🇺🇸 United States

ANKYLOS®

DI: 07392532221941 · Model: 31047122 · Dentsply Implants Manufacturing GmbH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
ANKYLOS®
Primary DI
07392532221941
Version / Model
31047122
Catalog Number
31047122
Company Name
Dentsply Implants Manufacturing GmbH
Labeler DUNS
344038836
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-11-18
Public Version
1
Public Version Date
2020-11-26
Public Version Status
New
Public Device Record Key
5f7f39a6-f184-48f8-b7a6-ad2d37a0fa95

Device Description

Regular C/X 3-in-1 Cap 15°

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
High-level Disinfectant

Product Codes

Code Name
DZE IMPLANT, ENDOSSEOUS, ROOT-FORM

GMDN Terms

Code Name
44880 Dental implant suprastructure, temporary, preformed, single-use

Identifiers

Type ID
Previous EFRI310471222
Primary 07392532221941

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Storage, in the original packaging, at room temperature in a dry place away from sunlight.