FDA UDI In Commercial Distribution 🇺🇸 United States

3M™

DI: 10707387802919 · Model: 8180F · 3M COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
5

Basic Information

Brand Name
3M™
Primary DI
10707387802919
Version / Model
8180F
Catalog Number
8180F
Company Name
3M COMPANY
Labeler DUNS
830016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2022-09-23
Public Version
1
Public Version Date
2022-10-03
Public Version Status
New
Public Device Record Key
165cdb2b-130f-4a4f-a87a-4d92b9f3bbaf

Device Description

3M™ Electrosurgical Pad, 8180F, Large Split Non-Corded, 5 Each/Bag, 5 Bag/Pack, 8 Pack/Case, for Stryker

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
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
Package 04064035032814
Primary 10707387802919
Package 04064035032821
Unit of Use 04064035042134

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K833364 000