FDA UDI Not in Commercial Distribution 🇺🇸 United States

EPAD

DI: 00851641007084 · Model: EPAD · SAFEOP SURGICAL, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EPAD
Primary DI
00851641007084
Version / Model
EPAD
Catalog Number
100023
Company Name
SAFEOP SURGICAL, INC.
Labeler DUNS
078641162
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-14
Public Version
3
Public Version Date
2021-08-30
Public Version Status
Update
Public Device Record Key
f611b856-0879-4d71-8c84-bc15bde69cd6
Distribution End Date
2019-10-10

Device Description

Acquisition red left long cable

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
Yes
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
No

Product Codes

Code Name
IKN Electromyograph, Diagnostic
GWF Stimulator, Electrical, Evoked Response

GMDN Terms

Code Name
11614 Evoked-potential graphic recording system

Identifiers

Type ID
Primary 00851641007084

Customer Contacts

Phone
4107739601