FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00817617022338 · Model: 14759 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00817617022338
Version / Model
14759
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-02-06
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
6acb16c9-21a7-4adf-8083-60b2c0ad9bae

Device Description

Curaplex Nasogastric Tube, 14Fr 280ea/cs

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
KNT TUBES, GASTROINTESTINAL (AND ACCESSORIES)

GMDN Terms

Code Name
14221 Nasogastric feeding tube

Identifiers

Type ID
Package 00817617021430
Primary 00817617022338
Package 00817617021898

Device Sizes

Type Value Unit Text
Catheter Gauge 14 French