FDA UDI In Commercial Distribution 🇺🇸 United States

Zenith

DI: 00840067102510 · Model: 190307-200 · CADWELL INDUSTRIES, INC.
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Zenith
Primary DI
00840067102510
Version / Model
190307-200
Company Name
CADWELL INDUSTRIES, INC.
Labeler DUNS
098554157
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-04-15
Public Version
2
Public Version Date
2022-11-28
Public Version Status
Update
Public Device Record Key
52abf964-b13b-47c4-b26e-5f50e5d6ff6b

Device Description

Amplifier 144 Ch. Zenith

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GWF STIMULATOR, ELECTRICAL, EVOKED RESPONSE
GYC ELECTRODE, CORTICAL
ETN STIMULATOR, NERVE
GWG Endoscope, neurological

GMDN Terms

Code Name
11467 Electroencephalograph

Identifiers

Type ID
Primary 00840067102510

Customer Contacts