FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00810071632075 · Model: 8600-01482 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
3
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Curaplex
Primary DI
00810071632075
Version / Model
8600-01482
Catalog Number
8600-01482
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-09-30
Public Version
1
Public Version Date
2021-10-08
Public Version Status
New
Public Device Record Key
74f43f32-23d4-43a7-bf9c-39d7f30c567f

Device Description

*Custom* COVID20 PPE 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
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LYU ACCESSORY, SURGICAL APPAREL

GMDN Terms

Code Name
17983 Infectious waste spill kit
35452 Isolation gown, reusable
35492 Isolation gown, single-use

Identifiers

Type ID
Primary 00810071632075