FDA UDI In Commercial Distribution 🇺🇸 United States

PRO-FLOW

DI: 00606959032378 · Model: PRO-FLOW NASAL CANNULA, M-F, 0.45 x 0.40, SINGLE · Respironics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PRO-FLOW
Primary DI
00606959032378
Version / Model
PRO-FLOW NASAL CANNULA, M-F, 0.45 x 0.40, SINGLE
Catalog Number
1097344
Company Name
Respironics, Inc.
Labeler DUNS
080728314
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-05
Public Version
5
Public Version Date
2021-02-26
Public Version Status
Update
Public Device Record Key
e5f7c212-0ef3-4329-822c-a13f1874e227

Device Description

PRO-FLOW NASAL CANNULA, M-F, 0.45 x 0.40, SINGLE

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
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
OLV Standard polysomnograph with electroencephalograph

GMDN Terms

Code Name
33843 Polysomnograph

Identifiers

Type ID
Package 30606959032379
Primary 00606959032378

Customer Contacts