FDA UDI In Commercial Distribution 🇺🇸 United States

Axiom®

DI: M6651018250 · Model: 101825 · AXIOM MEDICAL, INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Axiom®
Primary DI
M6651018250
Version / Model
101825
Company Name
AXIOM MEDICAL, INCORPORATED
Labeler DUNS
094439676
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
4
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
e0bdd410-9c0e-4682-9294-6fa2ca48a023

Device Description

Penrose Tubing, Silicone

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
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KDH Catheter (Gastric, Colonic, Etc.), Irrigation And Aspiration

GMDN Terms

Code Name
43437 Surgical capillary wound drain, luminal, synthetic polymer

Identifiers

Type ID
Package M6651018253
Package M6651018251
Primary M6651018250

Customer Contacts

Phone
310-533-9020

Premarket Submissions

Submission Number Supplement Number
K781749 000

Device Sizes

Type Value Unit Text
Length 18 Inch
Lumen/Inner Diameter 0.25 Inch