FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00812277038033 · Model: 1071-17367 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00812277038033
Version / Model
1071-17367
Catalog Number
1071-17367
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
e6dea26f-822a-4a63-bfe4-7af65e7f49b1

Device Description

Curaplex Multi-Purpose Collection Bag with Hook 12/PK 40PK/CS

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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 00812277039290
Primary 00812277038033
Package 00810071630552