FDA UDI In Commercial Distribution 🇺🇸 United States

PROGREAT

DI: 04987350738141 · Model: MC*PC2013ZRC · TERUMO CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PROGREAT
Primary DI
04987350738141
Version / Model
MC*PC2013ZRC
Catalog Number
MC*PC2013ZRC
Company Name
TERUMO CORPORATION
Labeler DUNS
690543319
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-09-06
Public Version
1
Public Version Date
2021-09-14
Public Version Status
New
Public Device Record Key
b1f313c3-0771-444a-ab62-be2a2be42234

Device Description

PROGREAT Microcatheter System

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
KRA Catheter, continuous flush
DQO Catheter, intravascular, diagnostic

GMDN Terms

Code Name
10691 Vascular microcatheter

Identifiers

Type ID
Primary 04987350738141
Package 54987350738146

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 0.67 Millimeter
Length 130 Centimeter
Lumen/Inner Diameter 0.49 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Fragile. Keep dry. Keep away from sunlight. Stacking limit by 10.