FDA UDI In Commercial Distribution 🇺🇸 United States

Curaplex

DI: 00810094574505 · Model: MD300CN310 · BOUND TREE MEDICAL, LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Curaplex
Primary DI
00810094574505
Version / Model
MD300CN310
Catalog Number
2711-30310
Company Name
BOUND TREE MEDICAL, LLC
Labeler DUNS
070556204
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-08
Public Version
2
Public Version Date
2023-02-06
Public Version Status
Update
Public Device Record Key
5be5399f-1d37-4a62-a70b-08d5b29bd1e7

Device Description

Pulse Oximeter Fingertip

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
Yes
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
MR Unsafe
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DQA Oximeter

GMDN Terms

Code Name
45607 Pulse oximeter

Identifiers

Type ID
Package 00810094574529
Package 00810094574512
Primary 00810094574505

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-25 – 70 Degrees Celsius