FDA UDI Not in Commercial Distribution 🇺🇸 United States

Boa®

DI: 00816849017600 · Model: DSO-013 · ENDOCHOICE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Boa®
Primary DI
00816849017600
Version / Model
DSO-013
Company Name
ENDOCHOICE, INC.
Labeler DUNS
014154279
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-09-08
Public Version
4
Public Version Date
2023-11-02
Public Version Status
Update
Public Device Record Key
6b1dcd27-657f-4b93-83b2-93729ae9322d
Distribution End Date
2018-12-31

Device Description

Polypectomy Snare, Stiff Wire

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FDI Snare, Flexible

GMDN Terms

Code Name
38719 Polypectomy endoscopic ligator, single-use

Identifiers

Type ID
Primary 00816849017600
Unit of Use 00816849017594

Customer Contacts

Phone
888-632-3636