FDA UDI In Commercial Distribution 🇺🇸 United States

CODMAN®

DI: 10381780513612 · Model: 261223 · INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CODMAN®
Primary DI
10381780513612
Version / Model
261223
Catalog Number
26-1223
Company Name
INTEGRA LIFESCIENCES PRODUCTION CORPORATION
Labeler DUNS
081277700
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-01
Public Version
5
Public Version Date
2023-04-14
Public Version Status
Update
Public Device Record Key
06fdc594-1e54-498a-a566-84a2a6505a43

Device Description

CODMAN® Disposable Perforator 9mm

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
HBF DRILLS, BURRS, TREPHINES & ACCESSORIES (COMPOUND, POWERED)

GMDN Terms

Code Name
46277 Automatic cranial perforator, single-use

Identifiers

Type ID
Primary 10381780513612

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K071931 000

Device Sizes

Type Value Unit Text
Outer Diameter 9 Millimeter