FDA UDI In Commercial Distribution 🇺🇸 United States

Zethon

DI: 05059358044643 · Model: 104184 · ZETHON LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Zethon
Primary DI
05059358044643
Version / Model
104184
Company Name
ZETHON LIMITED
Labeler DUNS
774901748
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-22
Public Version
1
Public Version Date
2025-10-30
Public Version Status
New
Public Device Record Key
aca46030-6d29-4d28-b427-4f3def93aafa

Device Description

LEVER - HEKA

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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece

GMDN Terms

Code Name
47864 Surgical power tool hand-switch

Identifiers

Type ID
Primary 05059358044643

Premarket Submissions

Submission Number Supplement Number
K233958 000