FDA UDI In Commercial Distribution 🇺🇸 United States

spECTrum

DI: 00861539000103 · Model: 5000DQ · MECTA CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
spECTrum
Primary DI
00861539000103
Version / Model
5000DQ
Company Name
MECTA CORPORATION
Labeler DUNS
037079324
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-24
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
f65b3129-aafb-4660-aeb0-31ce90dd9746

Device Description

100 Joule ECT Device with 4 Parameter Setting Controls and Patient Monitoring

Device Characteristics

Single Use
No
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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GXC Device, Electroconvulsive Therapy

GMDN Terms

Code Name
11484 Electroconvulsive therapy system

Identifiers

Type ID
Primary 00861539000103

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K965070 000