FDA UDI In Commercial Distribution 🇺🇸 United States

72" 22MM ULTRA FLEX® TUBING

DI: 00612649193458 · Model: 837-101-150F · King Systems Corporation
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
72" 22MM ULTRA FLEX® TUBING
Primary DI
00612649193458
Version / Model
837-101-150F
Catalog Number
837-101-150F
Company Name
King Systems Corporation
Labeler DUNS
009299017
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-13
Public Version
1
Public Version Date
2022-12-21
Public Version Status
New
Public Device Record Key
ab97dfb7-aec0-456d-9221-8ddcd0791ec4

Device Description

TUBING,22F,75" SEGMENTED @12"

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
BYX TUBING, PRESSURE AND ACCESSORIES

GMDN Terms

Code Name
45566 Gas-sampling/monitoring respiratory tubing, single-use

Identifiers

Type ID
Package 00612649178707
Primary 00612649193458

Customer Contacts

Phone
+14107686464