FDA UDI In Commercial Distribution 🇺🇸 United States

Bowman Perfusion Monitor, 240V

DI: B238H000107110 · Model: Model 500 · HEMEDEX, INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Bowman Perfusion Monitor, 240V
Primary DI
B238H000107110
Version / Model
Model 500
Catalog Number
H0001-0711
Company Name
HEMEDEX, INC
Labeler DUNS
128045676
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-21
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
017c51b0-8db9-45f2-95fa-d72cc5d75662

Device Description

Perfusion Monitor, 240V

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
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
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DPW Flowmeter, Blood, Cardiovascular

GMDN Terms

Code Name
45552 Patient monitoring system module, intracranial pressure

Identifiers

Type ID
Primary B238H000107110

Premarket Submissions

Submission Number Supplement Number
K013376 000