FDA UDI In Commercial Distribution 🇺🇸 United States

COLUMBUS REVISION

DI: 04046963850319 · Model: NQ729 · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
COLUMBUS REVISION
Primary DI
04046963850319
Version / Model
NQ729
Catalog Number
NQ729
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-08
Public Version
5
Public Version Date
2023-08-25
Public Version Status
Update
Public Device Record Key
66e78f05-b26e-4ca7-bf88-a1038fc07da0

Device Description

COLUMBUS REV FEM.SPACER PLATE F4 15MM

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
Yes
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 04046963850319

Customer Contacts