FDA UDI In Commercial Distribution 🇺🇸 United States

Ligation Device

DI: 06923646508720 · Model: Loop20B0-LD230D0 · Leo Medical Co., Ltd.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ligation Device
Primary DI
06923646508720
Version / Model
Loop20B0-LD230D0
Catalog Number
Loop20B0-LD230D0
Company Name
Leo Medical Co., Ltd.
Labeler DUNS
421371962
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-01-04
Public Version
1
Public Version Date
2026-01-12
Public Version Status
New
Public Device Record Key
2be888ec-0c96-4b1d-aed0-e0a2d5d30cba

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FHN Ligator, Hemorrhoidal
MND Ligator, Esophageal

GMDN Terms

Code Name
38719 Polypectomy endoscopic ligator, single-use

Identifiers

Type ID
Primary 06923646508720

Premarket Submissions

Submission Number Supplement Number
K172985 000