FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00817617020815 · Model: 2114-16304 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00817617020815
Version / Model
2114-16304
Catalog Number
2114-16304
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-27
Public Version
3
Public Version Date
2019-09-10
Public Version Status
Update
Public Device Record Key
c79f27e5-2e4b-4da0-b42b-c11b96432c34

Device Description

Curaplex PVC LMA, Size 4

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
No

Product Codes

Code Name
CAE AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY

GMDN Terms

Code Name
45036 Laryngeal mask airway, single-use

Identifiers

Type ID
Package 00817617020839
Package 00817617020822
Primary 00817617020815

Device Sizes

Type Value Unit Text
Device Size Text, specify Adult 50 to 70kg