FDA UDI In Commercial Distribution 🇺🇸 United States

Guide Pin

DI: 00813110029454 · Model: 260-101-280 · BICON, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
4

Basic Information

Brand Name
Guide Pin
Primary DI
00813110029454
Version / Model
260-101-280
Catalog Number
260-101-280
Company Name
BICON, LLC
Labeler DUNS
945015758
Distribution Status
In Commercial Distribution
Device Count in Pkg
4
Record Status
Published
Publish Date
2022-09-19
Public Version
1
Public Version Date
2022-09-27
Public Version Status
New
Public Device Record Key
1adc262c-c596-4531-86cc-43512d066707

Device Description

2.0mm Guide Pin - Tall Post (4)

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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
NDP Accessories, Implant, Dental, Endosseous

GMDN Terms

Code Name
44879 Dental implant suprastructure, permanent, preformed

Identifiers

Type ID
Unit of Use 10813110024234
Primary 00813110029454

Customer Contacts

Phone
617-524-4443