FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00810071633607 · Model: 1071-11106 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
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
00810071633607
Version / Model
1071-11106
Catalog Number
1071-11106
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
1
Public Version Date
2023-01-09
Public Version Status
New
Public Device Record Key
9847f816-ec70-48bd-ac48-a35c14f08516

Device Description

CURAPLEX DISPENSER FOR EMESIS BAG, HOLDS 25 6EA/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
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
FNY BASIN, EMESIS

GMDN Terms

Code Name
36258 Emesis bag

Identifiers

Type ID
Package 00810071633737
Primary 00810071633607
Package 00810071633805