FDA UDI In Commercial Distribution 🇺🇸 United States

Protekt Pulse

DI: 05060488570315 · Model: 20110 · PROACTIVE MEDICAL PRODUCTS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Protekt Pulse
Primary DI
05060488570315
Version / Model
20110
Catalog Number
20110
Company Name
PROACTIVE MEDICAL PRODUCTS, LLC
Labeler DUNS
078582655
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-12
Public Version
3
Public Version Date
2021-11-10
Public Version Status
Update
Public Device Record Key
dfdd1871-5ab3-42c5-af99-4861877f9d63

Device Description

FINGER PULSE OXIMETER

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
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
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
Primary 05060488570315

Customer Contacts

Device Sizes

Type Value Unit Text
Width 2.5 Inch
Length 1 Inch
Height 1 Inch