FDA UDI In Commercial Distribution 🇺🇸 United States

CRANIALMAP

DI: 07613327327151 · Model: 81-81037 · Stryker Leibinger GmbH & Co. KG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CRANIALMAP
Primary DI
07613327327151
Version / Model
81-81037
Catalog Number
81-81037
Company Name
Stryker Leibinger GmbH & Co. KG
Labeler DUNS
316153956
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-03-10
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
97cda470-4885-4d12-a209-2c947fe28d40

Device Description

CRANIALMAP PLANNING SALES DEMO

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
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HAW Neurological stereotaxic Instrument

GMDN Terms

Code Name
61496 Surgical planning/navigation-enhancement system

Identifiers

Type ID
Primary 07613327327151