FDA UDI In Commercial Distribution 🇺🇸 United States

N/A

DI: 00643169589834 · Model: 7372555 · MEDTRONIC SOFAMOR DANEK, INC.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00643169589834
Version / Model
7372555
Company Name
MEDTRONIC SOFAMOR DANEK, INC.
Labeler DUNS
830350380
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-05-21
Public Version
1
Public Version Date
2022-05-30
Public Version Status
New
Public Device Record Key
8b8468d0-e4a2-4742-85a0-c5ec5f3ed0d8

Device Description

TEMPLATE 7372555 55MM PLATE TEMPLATE

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
KWQ Appliance, fixation, spinal intervertebral body
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
HWT TEMPLATE

GMDN Terms

Code Name
46479 Surgical implant template, reusable

Identifiers

Type ID
Primary 00643169589834

Customer Contacts

Device Sizes

Type Value Unit Text
Length 55.0 Millimeter