FDA UDI In Commercial Distribution 🇺🇸 United States

CODMAN CERTAS®

DI: 10381780521334 · Model: 828859 · Integra LifeSciences Switzerland Sàrl
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
CODMAN CERTAS®
Primary DI
10381780521334
Version / Model
828859
Catalog Number
82-8859
Company Name
Integra LifeSciences Switzerland Sàrl
Labeler DUNS
480186617
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
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
9bd86e5a-8c5d-4c36-b5eb-a978ce583f22

Device Description

CODMAN® CERTAS® X-Ray Overlay Tool

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
JXG Shunt, central nervous system and components

GMDN Terms

Code Name
44856 Cerebrospinal fluid shunt valve programmer

Identifiers

Type ID
Unit of Use 00381780521337
Primary 10381780521334

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K143111 000