FDA UDI In Commercial Distribution 🇺🇸 United States

Lighted MicroLoop® Clinic Pack

DI: 00859911004627 · Model: 2202 · Bionix, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
200

Basic Information

Brand Name
Lighted MicroLoop® Clinic Pack
Primary DI
00859911004627
Version / Model
2202
Catalog Number
2202
Company Name
Bionix, LLC
Labeler DUNS
117844489
Distribution Status
In Commercial Distribution
Device Count in Pkg
200
Record Status
Published
Publish Date
2021-12-10
Public Version
3
Public Version Date
2023-07-17
Public Version Status
Update
Public Device Record Key
5ab99580-058d-423f-8629-16ccd7ec0efc

Device Description

Clinic Pack: Lighted MicroLoop Curette

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
Yes
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
JYG CURETTE, EAR

GMDN Terms

Code Name
65446 ENT illuminating foreign body extraction set

Identifiers

Type ID
Unit of Use 10859911004624
Primary 00859911004627

Customer Contacts