FDA UDI In Commercial Distribution 🇺🇸 United States

STEIGMANN-GOFF BANDITO

DI: 30653405053679 · Model: 100225 · Conmed Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
STEIGMANN-GOFF BANDITO
Primary DI
30653405053679
Version / Model
100225
Catalog Number
100225
Company Name
Conmed Corporation
Labeler DUNS
071595540
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2016-09-24
Public Version
3
Public Version Date
2023-09-04
Public Version Status
Update
Public Device Record Key
671cd427-f784-4121-b64a-5910fef967c4

Device Description

STIEGMANN-GOFF BANDITO ENDOSCOPIC LIGATOR

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FHN Ligator, hemorrhoidal

GMDN Terms

Code Name
46680 Oesophageal endoscopic ligator, single-use

Identifiers

Type ID
Package 20653405053672
Primary 30653405053679
Unit of Use 00653405053678

Customer Contacts