FDA UDI In Commercial Distribution 🇺🇸 United States

O2-MAX

DI: 00841470101510 · Model: 313-7555X · PULMODYNE INC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
O2-MAX
Primary DI
00841470101510
Version / Model
313-7555X
Company Name
PULMODYNE INC
Labeler DUNS
030619483
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-30
Public Version
5
Public Version Date
2019-11-11
Public Version Status
Update
Public Device Record Key
3ffa63e7-c8a1-4e84-85d7-f696813b521e

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
BYE Attachment, Breathing, Positive End Expiratory Pressure

GMDN Terms

Code Name
37498 Respiratory oxygen therapy system

Identifiers

Type ID
Package 10841470101517
Primary 00841470101510

Customer Contacts

Phone
313-246-5505

Device Sizes

Type Value Unit Text
Device Size Text, specify 5.0/7.5/10.0cm
Device Size Text, specify Adult Large