FDA UDI Not in Commercial Distribution 🇺🇸 United States

ANKYLOS®

DI: EFRI310210202 · Model: 31021020 · Dentsply Implants Manufacturing GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ANKYLOS®
Primary DI
EFRI310210202
Version / Model
31021020
Catalog Number
31021020
Company Name
Dentsply Implants Manufacturing GmbH
Labeler DUNS
344038836
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
8
Public Version Date
2020-12-07
Public Version Status
Update
Public Device Record Key
5ae18fa5-f807-4e00-a462-2d2e95bc07f9
Distribution End Date
2020-12-07

Device Description

Sulcus Former for Standard Abutments a/3.0

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
Moist Heat or Steam Sterilization

Product Codes

Code Name
DZE IMPLANT, ENDOSSEOUS, ROOT-FORM

GMDN Terms

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

Identifiers

Type ID
Primary EFRI310210202

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.