FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653206773 · Model: NK047K · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04038653206773
Version / Model
NK047K
Catalog Number
NK047K
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
5f031251-9125-4e6d-84c9-3d3021815487

Device Description

BIPOLAR CUP ID28MM OD47MM SELF-CENTERING

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
KWY Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented

GMDN Terms

Code Name
33695 Bipolar femoral head outer component, hemiarthroplasty

Identifiers

Type ID
Primary 04038653206773

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Inner diameter (mm) : 28.000 MM
Device Size Text, specify Outer diameter (mm) : 47.000 MM