FDA UDI Not in Commercial Distribution 🇺🇸 United States

AF811

DI: 00606959042407 · Model: AF811 w/Filtered Exhal Port Procedure Pack, Sm SA · Respironics, Inc.
Product Codes
2
GMDN Terms
2
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
AF811
Primary DI
00606959042407
Version / Model
AF811 w/Filtered Exhal Port Procedure Pack, Sm SA
Catalog Number
1130109
Company Name
Respironics, Inc.
Labeler DUNS
080728314
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-22
Public Version
6
Public Version Date
2022-10-24
Public Version Status
Update
Public Device Record Key
2ffa5a96-250f-4aa0-b9ec-b880a846d955
Distribution End Date
2021-03-05

Device Description

Philips Procedure, AF811 with Filtered Exhalation Port, Small, 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
57813 CPAP/BPAP face mask, single-use
37706 Ventilator breathing circuit, single-use

Identifiers

Type ID
Package 30606959042408
Primary 00606959042407

Customer Contacts

Storage Conditions

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