FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00810071631825 · Model: 5207F-SE-E · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
25

Basic Information

Brand Name
Curaplex
Primary DI
00810071631825
Version / Model
5207F-SE-E
Catalog Number
301-5207F-SE-E
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
25
Record Status
Published
Publish Date
2021-09-30
Public Version
2
Public Version Date
2022-03-22
Public Version Status
Update
Public Device Record Key
501a8bc9-71f3-49c8-85f9-47ed6a3ef6e2

Device Description

PEDIATRIC 7FT ETCO2/O2 CANNULA w/FITS-ALL, Reflective Connector - EXTENDED

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
No
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
CCK ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE

GMDN Terms

Code Name
36306 Nasal oxygen cannula, carbon-dioxide-sampling

Identifiers

Type ID
Unit of Use 00810071631733
Primary 00810071631825

Premarket Submissions

Submission Number Supplement Number
K063813 000

Device Sizes

Type Value Unit Text
Length 14 Feet
Device Size Text, specify Pediatric 7' EXTENDED

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
General Warehouse