FDA UDI In Commercial Distribution 🇺🇸 United States

E.MOTION PS/REVISION

DI: 04038653443253 · Model: NE181R · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
E.MOTION PS/REVISION
Primary DI
04038653443253
Version / Model
NE181R
Catalog Number
NE181R
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-23
Public Version
2
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
f6d4af64-09d2-4def-b521-0dff1eaeeb19

Device Description

E.MOTION PS SCREW DRIVER SW3.0

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
HXX SCREWDRIVER

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 04038653443253

Customer Contacts