FDA UDI In Commercial Distribution 🇺🇸 United States

CODMAN®

DI: 10381780520511 · Model: 826642 · INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CODMAN®
Primary DI
10381780520511
Version / Model
826642
Catalog Number
82-6642
Company Name
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Labeler DUNS
081277700
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-02-28
Public Version
6
Public Version Date
2023-04-14
Public Version Status
Update
Public Device Record Key
b5520c6a-d752-454a-9711-11f5fd1c5dd1

Device Description

CODMAN® SIEMENS 10 Pin Interface Cable

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GWM Device, monitoring, intracranial pressure

GMDN Terms

Code Name
47487 Electrical-only medical device connection cable, reusable

Identifiers

Type ID
Primary 10381780520511

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K945585 000