FDA UDI In Commercial Distribution 🇺🇸 United States

Biolox® delta

DI: 04046963190484 · Model: NK563D · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Biolox® delta
Primary DI
04046963190484
Version / Model
NK563D
Catalog Number
NK563D
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
3
Public Version Date
2020-09-09
Public Version Status
Update
Public Device Record Key
f568c151-1d9e-4833-948b-1b33d221e9ff

Device Description

BIOLOX DELTA PROSTH.HEAD 12/14 32MM XL

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
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented

GMDN Terms

Code Name
38156 Ceramic femoral head prosthesis

Identifiers

Type ID
Primary 04046963190484

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Neck length : + 7.0
Device Size Text, specify Outer diameter (mm) : 32.000 MM
Device Size Text, specify Figure / Size : Size XL
Device Size Text, specify Taper Size : 12/14