FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00817617023090 · Model: 533-MS-YK10EA · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00817617023090
Version / Model
533-MS-YK10EA
Catalog Number
533-MS-YK10EA
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-04
Public Version
5
Public Version Date
2021-06-08
Public Version Status
Update
Public Device Record Key
ff0063d7-eb73-48a9-8d2e-cc736e5a2260

Device Description

Yankaeur Tip only, Vented

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
No
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
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
GCX APPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED

GMDN Terms

Code Name
16779 Suction/irrigation tubing, single-use

Identifiers

Type ID
Package 00817617023571
Primary 00817617023090