FDA UDI In Commercial Distribution 🇺🇸 United States

PFM

DI: 05099169439849 · Model: 4300 · VITALOGRAPH (IRELAND) LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
PFM
Primary DI
05099169439849
Version / Model
4300
Company Name
VITALOGRAPH (IRELAND) LIMITED
Labeler DUNS
219683489
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-08
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
64dd50a5-788a-4ee5-a15e-d02b3a9b2081

Device Description

4300 PEAK FLOW METER myPEF

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BXW CALIBRATOR, VOLUME, GAS

GMDN Terms

Code Name
46872 Peak flow meter, manual

Identifiers

Type ID
Package 35099169439840
Primary 05099169439849
Package 55099169439844

Premarket Submissions

Submission Number Supplement Number
K781922 000

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
10 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
0 – 50 Degrees Celsius