FDA UDI In Commercial Distribution 🇺🇸 United States

FINECROSS

DI: 04987892058875 · Model: M3-1430 · TERUMO CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
FINECROSS
Primary DI
04987892058875
Version / Model
M3-1430
Catalog Number
NC*A853B
Company Name
TERUMO CORPORATION
Labeler DUNS
690543319
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-06-20
Public Version
1
Public Version Date
2022-06-28
Public Version Status
New
Public Device Record Key
7c879202-5151-4ed1-bad9-ba455cae87d0

Device Description

FineCross M3 Coronary Micro-Guide Catheter

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
MR Unsafe
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
Package 54987892058870
Primary 04987892058875

Customer Contacts

Device Sizes

Type Value Unit Text
Length 130 Centimeter
Outer Diameter 0.61 Millimeter
Outer Diameter 0.84 Millimeter
Device Size Text, specify Clinically Relevant Size 1 is relative to catheter distal part. Clinically Relevant Size 2 is relative to catheter proximal part.

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Fragile. Keep dry. Keep away from sunlight. Stacking limit by 9.