FDA UDI Not in Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653107582 · Model: LX951S · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
AESCULAP
Primary DI
04038653107582
Version / Model
LX951S
Catalog Number
LX951S
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-10-10
Public Version
6
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
f5ddd5aa-a822-48c7-ae25-e66cbc301843
Distribution End Date
2021-05-03

Device Description

KIRSCHNER BORING WIRE 1.6X102MM DBL.TROC

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
35685 Orthopaedic bone wire

Identifiers

Type ID
Primary 04038653107582
Unit of Use 04038653340392

Customer Contacts