FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00817617021386 · Model: 8600-01181 · BOUND TREE MEDICAL, LLC
Product Codes
2
GMDN Terms
4
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00817617021386
Version / Model
8600-01181
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
7
Public Version Date
2024-01-03
Public Version Status
Update
Public Device Record Key
63fb4619-e9fb-4615-afc8-9ca2ea1162eb

Device Description

*Custom* City of Joliet Chest Decompression Kit

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
FOZ Catheter,intravascular,therapeutic,short-term less than 30 days
KDQ BOTTLE, COLLECTION, VACUUM

GMDN Terms

Code Name
47011 First aid absorbent pad/bandage
13913 Antiseptic skin swab
48131 Non-woven gauze pad
37482 Pleural catheter

Identifiers

Type ID
Primary 00817617021386