FDA UDI In Commercial Distribution 🇺🇸 United States

Resp-O2 Closed Suction Endotracheal Catheter

DI: 00840117305779 · Model: 31021 · DYNAREX CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Resp-O2 Closed Suction Endotracheal Catheter
Primary DI
00840117305779
Version / Model
31021
Company Name
DYNAREX CORPORATION
Labeler DUNS
008124539
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2021-04-22
Public Version
1
Public Version Date
2021-04-30
Public Version Status
New
Public Device Record Key
c5e6717e-99be-4f21-ae86-db55c9d04101

Device Description

Resp-O2 Closed Suction Endotracheal Catheter 12FR w/ T-piece Adult/Pediatric

Device Characteristics

Single Use
Yes
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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
BSY Catheters, Suction, Tracheobronchial

GMDN Terms

Code Name
63465 Closed-suction breathing circuit connector/switch

Identifiers

Type ID
Package 00840117305915
Primary 00840117305779
Unit of Use 00840117319745