FDA UDI In Commercial Distribution 🇺🇸 United States

Emergence Cuff

DI: 00813110024916 · Model: 260-140-010 · BICON, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
4

Basic Information

Brand Name
Emergence Cuff
Primary DI
00813110024916
Version / Model
260-140-010
Catalog Number
260-140-010
Company Name
BICON, LLC
Labeler DUNS
945015758
Distribution Status
In Commercial Distribution
Device Count in Pkg
4
Record Status
Published
Publish Date
2016-05-06
Public Version
4
Public Version Date
2020-03-25
Public Version Status
Update
Public Device Record Key
b3e898c1-690f-4754-9303-046d50805600

Device Description

4.0mm Emergence Cuff

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 00813110024916
Unit of Use 10813110024913

Customer Contacts

Phone
617-524-4443