FDA UDI In Commercial Distribution 🇺🇸 United States

PRIMOPAC

DI: 10705032076722 · Model: CP0426 · CORDIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
PRIMOPAC
Primary DI
10705032076722
Version / Model
CP0426
Catalog Number
CP0426
Company Name
CORDIS CORPORATION
Labeler DUNS
806136177
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-02-26
Public Version
2
Public Version Date
2024-03-21
Public Version Status
Update
Public Device Record Key
fd60188e-1896-4cc8-a38f-8e3cbad80667

Device Description

CP ST+ 6 JR4, JL4,PIG 145, CSI AVANTI, GW

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
Yes
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
OEZ Cardiovascular Procedure Kit

GMDN Terms

Code Name
10688 Angiographic catheter, single-use

Identifiers

Type ID
Package 20705032076729
Primary 10705032076722