FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046963067359 · Model: FS617 · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
16

Basic Information

Brand Name
AESCULAP
Primary DI
04046963067359
Version / Model
FS617
Catalog Number
FS617
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
16
Record Status
Published
Publish Date
2016-09-23
Public Version
6
Public Version Date
2021-04-06
Public Version Status
Update
Public Device Record Key
9ef5fbca-2089-4616-8a72-6187512e6f9e

Device Description

ORTHOPILOT DISPOS.PASSIVE MARKER STERILE

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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HAW Neurological stereotaxic Instrument

GMDN Terms

Code Name
38723 Robotic surgical navigation system

Identifiers

Type ID
Primary 04046963067359
Unit of Use 04038653457304

Customer Contacts