FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00815277022040 · Model: 6840155C · BOUND TREE MEDICAL, LLC
Product Codes
10
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00815277022040
Version / Model
6840155C
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
5bfeb4c0-8db4-4bd4-93db-edd6ecaf809d

Device Description

Kit Contents Only Curaplex Pediatric Kit No Case

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
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
FMF Syringe, piston
FCG Biopsy needle
MHC PORT, INTRAOSSEOUS, IMPLANTED
BTM Ventilator, emergency, manual (resuscitator)
DXQ blood pressure cuff
MMK Container, sharps
OGK Orotrachael intubation guide kit
FOZ Catheter,intravascular,therapeutic,short-term less than 30 days
POQ Blood transfusion kit
BTR Tube, tracheal (w/wo connector)

GMDN Terms

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

Identifiers

Type ID
Primary 00815277022040