FDA UDI In Commercial Distribution 🇺🇸 United States

Avante/Pacific

DI: 06900234100245 · Model: NSPH3020 · Solaris Medical Technology, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
7
Pkg Device Count
1

Basic Information

Brand Name
Avante/Pacific
Primary DI
06900234100245
Version / Model
NSPH3020
Company Name
Solaris Medical Technology, Inc.
Labeler DUNS
527945351
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-01-20
Public Version
2
Public Version Date
2021-11-10
Public Version Status
Update
Public Device Record Key
54b6106d-2b14-4db8-a2dd-0c9826463040

Device Description

Philips Compatible Reusable SpO2 Adult Soft-Finger Sensor (3.0m cable)

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
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
37808 Pulse oximeter probe, reusable

Identifiers

Type ID
Primary 06900234100245
Package 16900234100242
Package 26900234100249
Package 36900234100246
Package 46900234100243
Package 56900234100240
Package 66900234100247

Premarket Submissions

Submission Number Supplement Number
K100077 000