FDA UDI In Commercial Distribution 🇺🇸 United States

ENDURO

DI: 04046963644437 · Model: NS229T · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ENDURO
Primary DI
04046963644437
Version / Model
NS229T
Catalog Number
NS229T
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-24
Public Version
2
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
4a958c8c-5f8f-4934-ac37-f124cc03dc13

Device Description

ENDURO TRIAL FEMUR STEM D20X157 CEMENTED

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
Yes
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HWT TEMPLATE

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 04046963644437

Customer Contacts