FDA UDI In Commercial Distribution 🇺🇸 United States

PF 6052 Segmental Pressure 3 Cuff Method Kit

DI: 07332834001124 · Model: PF 6052 · Perimed AB
Product Codes
0
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PF 6052 Segmental Pressure 3 Cuff Method Kit
Primary DI
07332834001124
Version / Model
PF 6052
Catalog Number
93-00226
Company Name
Perimed AB
Labeler DUNS
354765570
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-01-31
Public Version
1
Public Version Date
2023-02-08
Public Version Status
New
Public Device Record Key
4af20e7d-a9fb-4ea2-967f-f22ea38086b3

Device Description

PF 6052 Segmental Pressure 3 Cuff Method Kit

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
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

GMDN Terms

Code Name
60451 Laser Doppler blood flowmeter

Identifiers

Type ID
Primary 07332834001124

Premarket Submissions

Submission Number Supplement Number
K152930 000