FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00815277022149 · Model: 73320XL · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
6
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00815277022149
Version / Model
73320XL
Catalog Number
73320XL
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
9
Public Version Date
2023-12-06
Public Version Status
Update
Public Device Record Key
946fe3c7-e6bd-4a8a-9f51-a11ff217416b

Device Description

Curaplex Decontamination Personal Protection Kit, XL

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
OKH Body fluids barrier kit

GMDN Terms

Code Name
11961 Face splash shield, single-use
57794 Surgical/medical respirator, non-antimicrobial, single-use
60660 Nitrile examination/treatment glove, non-powdered, antimicrobial
58390 Visitor hygiene coverall
58376 Eye splash shield, single-use
15056 Shoe cover

Identifiers

Type ID
Primary 00815277022149
Package 00810094572037