FDA UDI Not in Commercial Distribution 🇺🇸 United States

PerforMax

DI: 00606959042445 · Model: PerforMax w/Filtered Exhal Port Procedure Pack, L · Respironics, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PerforMax
Primary DI
00606959042445
Version / Model
PerforMax w/Filtered Exhal Port Procedure Pack, L
Catalog Number
1130113
Company Name
Respironics, Inc.
Labeler DUNS
080728314
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-18
Public Version
4
Public Version Date
2021-03-05
Public Version Status
Update
Public Device Record Key
ebce9c34-896d-4f9e-b896-baa30e30d255
Distribution End Date
2021-03-05

Device Description

Philips Procedure, PerforMax with Filtered Exhalation Port, Large, SA

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
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
MNT VENTILATOR, CONTINUOUS, MINIMAL VENTILATORY SUPPORT,FACILITY USE
BZD VENTILATOR, NON-CONTINUOUS (RESPIRATOR)

GMDN Terms

Code Name
57814 CPAP/BPAP face mask, reusable

Identifiers

Type ID
Package 30606959042446
Primary 00606959042445

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-4 – 140 Degrees Fahrenheit
Type
Storage Environment Temperature
Temperature Range
-20 – 60 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
15 – 95 Percent (%) Relative Humidity