FDA UDI In Commercial Distribution 🇺🇸 United States

Model

DI: 00813110024657 · Model: 260-102-508 · BICON, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Model
Primary DI
00813110024657
Version / Model
260-102-508
Catalog Number
260-102-508
Company Name
BICON, LLC
Labeler DUNS
945015758
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-06-10
Public Version
4
Public Version Date
2019-11-08
Public Version Status
Update
Public Device Record Key
26eafc3b-1b98-4b70-932f-bb88affe9f01

Device Description

5.0 x 6.0mm Large Plastic Implant Replica

Device Characteristics

Single Use
No
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
No
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
44879 Dental implant suprastructure, permanent, preformed

Identifiers

Type ID
Primary 00813110024657

Customer Contacts

Phone
617-524-4443