FDA UDI Not in Commercial Distribution 🇺🇸 United States

Biolox® forte

DI: 04038653120055 · Model: NK560 · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Biolox® forte
Primary DI
04038653120055
Version / Model
NK560
Catalog Number
NK560
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
5
Public Version Date
2021-10-28
Public Version Status
Update
Public Device Record Key
0e502083-6129-4a29-b297-0e6cd88cbde8
Distribution End Date
2016-03-27

Device Description

BIOLOX PROSTHESIS HEAD 12/14 32MM S

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
LWJ Prosthesis, hip, semi-constrained, metal/polymer, uncemented

GMDN Terms

Code Name
38156 Ceramic femoral head prosthesis

Identifiers

Type ID
Primary 04038653120055

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Outer diameter (mm) : 32.000 MM
Device Size Text, specify Figure / Size : Size S
Device Size Text, specify Neck length : - 4.0
Device Size Text, specify Taper Size : 12/14