FDA UDI In Commercial Distribution 🇺🇸 United States

BIONIX DEVELOPMENT CORPORATION

DI: 00859911004306 · Model: SP-20911 · Bionix, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BIONIX DEVELOPMENT CORPORATION
Primary DI
00859911004306
Version / Model
SP-20911
Catalog Number
20911
Company Name
Bionix, LLC
Labeler DUNS
117844489
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-22
Public Version
6
Public Version Date
2023-07-18
Public Version Status
Update
Public Device Record Key
9478c8d2-0461-4de7-865f-97a7c9552cd7

Device Description

Sample-DeClogger 14-16 F/Blue

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
Yes
PM Exempt
No
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
KNT TUBES, GASTROINTESTINAL (AND ACCESSORIES)

GMDN Terms

Code Name
58939 Enteral feeding tube clearing kit

Identifiers

Type ID
Primary 00859911004306

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K905164 000