FDA UDI In Commercial Distribution 🇺🇸 United States

Guided Surgery

DI: 00813110028044 · Model: 260-920-005 · BICON, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
Guided Surgery
Primary DI
00813110028044
Version / Model
260-920-005
Catalog Number
260-920-005
Company Name
BICON, LLC
Labeler DUNS
945015758
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2019-02-06
Public Version
3
Public Version Date
2020-04-06
Public Version Status
Update
Public Device Record Key
6fea3148-314a-48ab-8333-911235900f50

Device Description

2.0mm Guided Surgery Rings

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
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
35095 Surgical drill guide, reusable

Identifiers

Type ID
Primary 00813110028044
Unit of Use 10813110028041

Customer Contacts

Phone
617-524-4443