FDA UDI In Commercial Distribution 🇺🇸 United States

Nebulizing Elbow

DI: 00606959034433 · Model: SE Nebulizing Elbow Kit, US · Respironics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Nebulizing Elbow
Primary DI
00606959034433
Version / Model
SE Nebulizing Elbow Kit, US
Catalog Number
1120425
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
4
Public Version Date
2021-03-01
Public Version Status
Update
Public Device Record Key
a3dfd862-cbc6-423f-8a28-336d2d30b878

Device Description

SE Nebulizing Elbow Kit, Single, USA

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
CAF NEBULIZER (DIRECT PATIENT INTERFACE)

GMDN Terms

Code Name
57813 CPAP/BPAP face mask, single-use

Identifiers

Type ID
Package 30606959034434
Primary 00606959034433

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K102240 000

Storage Conditions

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