FDA UDI In Commercial Distribution 🇺🇸 United States

CODMAN®

DI: 10381780521396 · Model: 831323 · INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
CODMAN®
Primary DI
10381780521396
Version / Model
831323
Catalog Number
83-1323
Company Name
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Labeler DUNS
081277700
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2020-04-01
Public Version
7
Public Version Date
2023-04-14
Public Version Status
Update
Public Device Record Key
1068b74e-39f7-4b63-8a24-d9a2ce4335d1

Device Description

CODMAN® Peel-Away Catheter Introducer 9Fr.

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GYK Instrument, shunt system implantation

GMDN Terms

Code Name
16763 Intracranial pressure monitor

Identifiers

Type ID
Unit of Use 00381780521399
Primary 10381780521396

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K883607 000

Device Sizes

Type Value Unit Text
Catheter Gauge 9 French