FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00815277020169 · Model: 14651 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
5
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00815277020169
Version / Model
14651
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
6
Public Version Date
2023-10-18
Public Version Status
Update
Public Device Record Key
7cdff174-543c-49c1-bdf2-f01a410aaff5

Device Description

Curaplex Infection Control Kit, Latex Free, incl Gloves, Gown, Mask w/Shield, Alcohol Wipe, BioBag

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
OKH Body fluids barrier kit

GMDN Terms

Code Name
60660 Nitrile examination/treatment glove, non-powdered, antimicrobial
17988 Antiseptic skin towelette
35492 Isolation gown, single-use
57794 Surgical/medical respirator, non-antimicrobial, single-use
62172 Laboratory waste receptacle IVD

Identifiers

Type ID
Primary 00815277020169