FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00815277023337 · Model: 16108 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00815277023337
Version / Model
16108
Catalog Number
16108
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-14
Public Version
3
Public Version Date
2023-12-06
Public Version Status
Update
Public Device Record Key
41ad5e2a-13a1-4750-991f-0e18aa323a95

Device Description

Curaplex Yankauer without Vent 20ea/pk

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
BYY TUBE, ASPIRATING, FLEXIBLE, CONNECTING

GMDN Terms

Code Name
35917 Surgical/emergency suction cannula, non-illuminating, single-use

Identifiers

Type ID
Package 00815277023344
Package 00815277025607
Primary 00815277023337