FDA UDI In Commercial Distribution 🇺🇸 United States

3M™

DI: 50707387462593 · Model: 9165 · 3M COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
40

Basic Information

Brand Name
3M™
Primary DI
50707387462593
Version / Model
9165
Catalog Number
9165
Company Name
3M COMPANY
Labeler DUNS
830016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
40
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2020-06-05
Public Version Status
Update
Public Device Record Key
6bf4f993-c296-4080-bfc1-2edda240954c

Device Description

9165 UNIVERSAL PATIENT PLATE

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
Yes
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
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
58494 Electrosurgical return electrode, single-use

Identifiers

Type ID
Primary 50707387462593
Unit of Use 00707387462598

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K974279 000