FDA UDI In Commercial Distribution 🇺🇸 United States

ANKYLOS®

DI: 07392532221033 · Model: 31045021 · Dentsply Implants Manufacturing GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ANKYLOS®
Primary DI
07392532221033
Version / Model
31045021
Catalog Number
31045021
Company Name
Dentsply Implants Manufacturing GmbH
Labeler DUNS
344038836
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-14
Public Version
1
Public Version Date
2022-07-22
Public Version Status
New
Public Device Record Key
1277f0a0-e75a-45e1-b9c4-c92d17225a51

Device Description

TransferCap (PC) Standard Abutment a/1.5/6.0 & a/3.0/6.0

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
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
44880 Dental implant suprastructure, temporary, preformed, single-use

Identifiers

Type ID
Primary 07392532221033