FDA UDI In Commercial Distribution 🇺🇸 United States

3M™

DI: 10707387462601 · Model: 9130F · 3M COMPANY
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
3M™
Primary DI
10707387462601
Version / Model
9130F
Catalog Number
9130F
Company Name
3M COMPANY
Labeler DUNS
830016148
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2016-11-01
Public Version
4
Public Version Date
2020-06-05
Public Version Status
Update
Public Device Record Key
977d0eeb-30b4-40a3-a0ef-3de33d031650

Device Description

9130F UNIV ELECTRO W/CRD 200PLT/CS

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 10707387462601
Unit of Use 00707387462567
Package 50707387462609

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K974553 000