FDA UDI In Commercial Distribution 🇺🇸 United States

BodyMed

DI: 00815991025181 · Model: BDMPULSEOX · BOXOUT, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
BodyMed
Primary DI
00815991025181
Version / Model
BDMPULSEOX
Catalog Number
BDMPULSEOX
Company Name
BOXOUT, LLC
Labeler DUNS
066689993
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-10-11
Public Version
1
Public Version Date
2024-10-21
Public Version Status
New
Public Device Record Key
2a62a53b-373d-4e4d-ae32-8b38fcc31ec0

Device Description

BodyMed Fingertip Pulse Oximeter, red LED display, 2 AAA batteries included

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OCH Oximeter, Infrared, Sporting, Aviation

GMDN Terms

Code Name
45607 Pulse oximeter

Identifiers

Type ID
Package 20815991025185
Primary 00815991025181

Customer Contacts

Phone
866-528-2152