FDA UDI In Commercial Distribution 🇺🇸 United States

Spirotrac

DI: 65099169686740 · Model: 7000 · VITALOGRAPH (IRELAND) LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
21
Pkg Device Count
1

Basic Information

Brand Name
Spirotrac
Primary DI
65099169686740
Version / Model
7000
Company Name
VITALOGRAPH (IRELAND) LIMITED
Labeler DUNS
219683489
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-14
Public Version
5
Public Version Date
2022-03-08
Public Version Status
Update
Public Device Record Key
a0dd213a-f7f4-4f0e-8eab-e0d6545b6df0

Device Description

68674 software

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
BZG SPIROMETER, DIAGNOSTIC

GMDN Terms

Code Name
13680 Diagnostic spirometer, professional

Identifiers

Type ID
Package 15099169676760
Primary 65099169686740
Package 05099169706064
Package 15099169676814
Package 05099169706118
Package 15099169676777
Package 05099169706071
Package 05099169706057
Package 15099169676753
Package 05099169706040
Package 05099169706026
Package 15099169676746
Package 05099169706125
Package 15099169676821
Package 15099169676722
Package 15099169676852
Package 15099169676715
Package 05099169706156
Package 05099169706019
Package 05099169706194
Package 15099169676890

Premarket Submissions

Submission Number Supplement Number
K141546 000