FDA UDI In Commercial Distribution 🇺🇸 United States

Marketlab Inc

DI: 00817517020762 · Model: 42468 · MARKETLAB INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
12

Basic Information

Brand Name
Marketlab Inc
Primary DI
00817517020762
Version / Model
42468
Catalog Number
42468
Company Name
MARKETLAB INC.
Labeler DUNS
848917027
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2018-11-16
Public Version
4
Public Version Date
2020-12-04
Public Version Status
Update
Public Device Record Key
1a61c0d5-4cec-4c4d-9aee-7cc24bfb6ad4

Device Description

30cc/24Fr 100% Silicone Foley Catheter PK12

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
Yes
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
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
FOZ Catheter, intravascular, therapeutic, short-term less than 30 days

GMDN Terms

Code Name
34917 Indwelling urethral drainage balloon catheter, non-antimicrobial

Identifiers

Type ID
Primary 00817517020762
Unit of Use 00817517021455

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K160235 000