FDA UDI In Commercial Distribution 🇺🇸 United States

CAMLOG® Bite registration post

DI: E219J214150001 · Model: J2141.5000 · ALTATEC GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CAMLOG® Bite registration post
Primary DI
E219J214150001
Version / Model
J2141.5000
Catalog Number
J2141.5000
Company Name
ALTATEC GmbH
Labeler DUNS
322018193
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-12-18
Public Version
1
Public Version Date
2023-12-26
Public Version Status
New
Public Device Record Key
d2ffadcc-02ed-4b95-833b-2fe70aa042e2

Device Description

CAMLOG® Bite registration post, incl. fixing screw and bite registration cap, Ø 5.0 mm, prosthetic height 8.1 mm, titanium alloy/PBT, sterile

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

Identifiers

Type ID
Primary E219J214150001

Customer Contacts

Phone
7609181857