FDA UDI In Commercial Distribution 🇺🇸 United States

B500 SERIES

DI: B5051017 · Model: B505-1017 · BETA BIOMED SERVICES INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
B500 SERIES
Primary DI
B5051017
Version / Model
B505-1017
Company Name
BETA BIOMED SERVICES INC
Labeler DUNS
959702788
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-15
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
eb28b68b-25f8-47bb-aba1-fbad3b70bab9

Device Description

B500 SERIES PULSE OXIMETER SENSOR

Device Characteristics

Single Use
No
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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
Yes
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
17148 Pulse oximeter, line-powered

Identifiers

Type ID
Package B505101703
Primary B5051017