FDA UDI In Commercial Distribution 🇺🇸 United States

Bite registration cap

DI: E219J211233001 · Model: J2112.3300 · ALTATEC GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Bite registration cap
Primary DI
E219J211233001
Version / Model
J2112.3300
Catalog Number
J2112.3300
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
1269c2e9-999d-4f45-b443-e90bbb31196c

Device Description

Bite registration cap (5 units) d 3.3 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
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 E219J211233001

Customer Contacts

Phone
7609181857