FDA UDI In Commercial Distribution 🇺🇸 United States

Causse

DI: 00681490034159 · Model: 1128450 · MEDTRONIC XOMED, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Causse
Primary DI
00681490034159
Version / Model
1128450
Company Name
MEDTRONIC XOMED, INC.
Labeler DUNS
835465063
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-06-23
Public Version
3
Public Version Date
2024-02-19
Public Version Status
Update
Public Device Record Key
2d53e594-5ad1-4aea-9226-23111d2d2d84

Device Description

IMPLANT 1128450 CAUSSE STAPES SHEET FLPL

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
MR Conditional
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
ETA REPLACEMENT, OSSICULAR PROSTHESIS, TOTAL

GMDN Terms

Code Name
45231 Silicone-sheet tissue reconstructive material, non-sterile

Identifiers

Type ID
Primary 00681490034159

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 15 MM X 8 MM