FDA UDI Not in Commercial Distribution 🇺🇸 United States

PF 5002 Basic Main Unit

DI: 07332834000417 · Model: PF 5002 · Perimed AB
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PF 5002 Basic Main Unit
Primary DI
07332834000417
Version / Model
PF 5002
Company Name
Perimed AB
Labeler DUNS
354765570
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-13
Public Version
4
Public Version Date
2023-02-01
Public Version Status
Update
Public Device Record Key
9bc90773-dbc9-49bf-aca3-55289965ba53
Distribution End Date
2023-02-01

Device Description

PF 5002 Basic Main Unit

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
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
46934 Transcutaneous blood gas monitoring system

Identifiers

Type ID
Primary 07332834000417

Premarket Submissions

Submission Number Supplement Number
K974285 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
0 – 50 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
30 – 85 Percent (%) Relative Humidity