FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653369355 · Model: FS877R · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
2

Basic Information

Brand Name
AESCULAP
Primary DI
04038653369355
Version / Model
FS877R
Catalog Number
FS877R
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2016-10-03
Public Version
5
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
63649a78-e1f9-42aa-a29a-10f7b1526c29

Device Description

ORTHOPILOT ACL GUIDE PINS W/SHARP TIP

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
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 04038653369355
Unit of Use 04038653332816

Customer Contacts