FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00810071635786 · Model: 1860-08705 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
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
00810071635786
Version / Model
1860-08705
Catalog Number
1860-08705
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-30
Public Version
2
Public Version Date
2023-08-18
Public Version Status
Update
Public Device Record Key
a925edd8-d3bb-4c27-871a-1dc56a927cfa

Device Description

Curaplex Sharps Container, 32 Quart 1EA 10EA/CS

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MMK Container, sharps

GMDN Terms

Code Name
35429 Sharps container

Identifiers

Type ID
Package 00810071635823
Primary 00810071635786

Premarket Submissions

Submission Number Supplement Number
K942054 000