FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00810094575908 · Model: 2010-36110 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
50

Basic Information

Brand Name
Curaplex
Primary DI
00810094575908
Version / Model
2010-36110
Catalog Number
2010-36110
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2023-08-30
Public Version
2
Public Version Date
2023-09-14
Public Version Status
Update
Public Device Record Key
1e9d10e5-eeb7-4255-88b3-b013d8b61813

Device Description

Curaplex® Guedel Airway, 110mm, Orange

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
Yes
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
No
Sterilization Prior Use
No

Product Codes

Code Name
CAE AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY

GMDN Terms

Code Name
42424 Oropharyngeal airway, single-use

Identifiers

Type ID
Package 00810094575922
Primary 00810094575908
Unit of Use 00810094576141