FDA UDI In Commercial Distribution 🇺🇸 United States

CODMAN®

DI: 10381780514367 · Model: 451068 · INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CODMAN®
Primary DI
10381780514367
Version / Model
451068
Catalog Number
45-1068
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
5
Public Version Date
2023-04-14
Public Version Status
Update
Public Device Record Key
477ca643-8faf-4116-9370-33d539b431a3

Device Description

CODMAN® PACE Ventricular Needle

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
Yes
PM Exempt
Yes
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HAO INSTRUMENT, SURGICAL, NON-POWERED

GMDN Terms

Code Name
61854 Intracerebral cannula, nonimplantable, reusable

Identifiers

Type ID
Primary 10381780514367

Customer Contacts