FDA UDI Not in Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046963138653 · Model: LT209T · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04046963138653
Version / Model
LT209T
Catalog Number
LT209T
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-30
Public Version
5
Public Version Date
2024-02-29
Public Version Status
Update
Public Device Record Key
cd747dfb-dec0-4c7f-8bdc-dcc7deb23fc9
Distribution End Date
2016-03-07

Device Description

SPACER 9MM W/FIXATION SCREW

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
HWC Screw, fixation, bone

GMDN Terms

Code Name
46647 Orthopaedic fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 04046963138653

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Height : 9.000 MM