FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00812277034172 · Model: 670178-KIT · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00812277034172
Version / Model
670178-KIT
Catalog Number
670178-KIT
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-02-10
Public Version
2
Public Version Date
2022-08-16
Public Version Status
Update
Public Device Record Key
8a6f64f8-578b-4cf8-b359-df8e17e0fab9

Device Description

Pediatric NPA kit (22-24 Fr)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BTQ AIRWAY, NASOPHARYNGEAL

GMDN Terms

Code Name
42422 Nasopharyngeal airway, single-use

Identifiers

Type ID
Primary 00812277034172
Package 00810094571184