FDA UDI In Commercial Distribution 🇺🇸 United States

ESI

DI: B3963708120 · Model: 37-0812 · FTT MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ESI
Primary DI
B3963708120
Version / Model
37-0812
Company Name
FTT MEDICAL, INC.
Labeler DUNS
002212793
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-22
Public Version
3
Public Version Date
2019-09-18
Public Version Status
Update
Public Device Record Key
cbf0a04a-8c42-4158-8f2d-69f966e60360

Device Description

LIGATING RINGS, PACKAGE OF 100. (Caution: This Product Contains Natural Rubber Latex Which May Cause Allergic Reactions)

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
FHN Ligator, Hemorrhoidal

GMDN Terms

Code Name
35157 Haemorrhoid ligator

Identifiers

Type ID
Primary B3963708120