FDA UDI In Commercial Distribution 🇺🇸 United States

ADROIT

DI: 20705032071663 · Model: 67201000 · Cordis US Corp.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
ADROIT
Primary DI
20705032071663
Version / Model
67201000
Catalog Number
67201000
Company Name
Cordis US Corp.
Labeler DUNS
118274128
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-28
Public Version
11
Public Version Date
2025-09-05
Public Version Status
Update
Public Device Record Key
a6859964-f6b2-4c71-994a-a4069b71bd9a

Device Description

6F .072 JL6 100 CM

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
DQY CATHETER, PERCUTANEOUS

GMDN Terms

Code Name
17846 Vascular guide-catheter, single-use

Identifiers

Type ID
Primary 20705032071663

Premarket Submissions

Submission Number Supplement Number
K131225 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius