FDA UDI In Commercial Distribution 🇺🇸 United States

PerforMax

DI: 00606959042452 · Model: PerforMax with FEP Procedure Pack, Small · Respironics, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PerforMax
Primary DI
00606959042452
Version / Model
PerforMax with FEP Procedure Pack, Small
Catalog Number
1130114
Company Name
Respironics, Inc.
Labeler DUNS
080728314
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-18
Public Version
3
Public Version Date
2021-03-02
Public Version Status
Update
Public Device Record Key
a5086bd3-23ac-4b41-968d-38a7dcdfaa64

Device Description

PerforMax with FEP Procedure Pack, Small

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
BZD VENTILATOR, NON-CONTINUOUS (RESPIRATOR)
MNT VENTILATOR, CONTINUOUS, MINIMAL VENTILATORY SUPPORT,FACILITY USE

GMDN Terms

Code Name
57814 CPAP/BPAP face mask, reusable

Identifiers

Type ID
Package 30606959042453
Primary 00606959042452

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