FDA UDI In Commercial Distribution 🇺🇸 United States

PFT

DI: 15099169284392 · Model: 2820 · VITALOGRAPH (IRELAND) LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
PFT
Primary DI
15099169284392
Version / Model
2820
Company Name
VITALOGRAPH (IRELAND) LIMITED
Labeler DUNS
219683489
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-01
Public Version
5
Public Version Date
2023-07-06
Public Version Status
Update
Public Device Record Key
26dc0abb-895f-4c84-b7c8-d72a717919bd

Device Description

2820 BVF(28365) + 2020 REAR BITE-ON + 2030 DISP NOSE CLIP

Device Characteristics

Single Use
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BZG SPIROMETER, DIAGNOSTIC

GMDN Terms

Code Name
44545 Breathing mouthpiece, single-use

Identifiers

Type ID
Package 05099169284395
Primary 15099169284392
Package 55099169284390

Premarket Submissions

Submission Number Supplement Number
K942779 000

Storage Conditions

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