FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00815277021234 · Model: 660222 · BOUND TREE MEDICAL, LLC
Product Codes
12
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00815277021234
Version / Model
660222
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-14
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
448caea0-125a-4aab-be08-c8559e6d150e

Device Description

ADVANCED TRAUMA KIT - US EMBASSY

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
Yes
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DQA Oximeter
MHC PORT, INTRAOSSEOUS, IMPLANTED
FOZ Catheter,intravascular,therapeutic,short-term less than 30 days
BTM Ventilator, emergency, manual (resuscitator)
POQ Blood transfusion kit
HEB TAMPON, MENSTRUAL, UNSCENTED
FRO Dressing, wound, drug
FMF Syringe, piston
DXQ blood pressure cuff
MMK Container, sharps
NBW SYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER
GAR Suture, nonabsorbable, synthetic, polyamide

GMDN Terms

Code Name
43000 First aid kit, non-medicated, reusable

Identifiers

Type ID
Primary 00815277021234