FDA UDI In Commercial Distribution 🇺🇸 United States

Gyrus ACMI

DI: 00821925038622 · Model: RKA-4 · Gyrus ACMI, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Gyrus ACMI
Primary DI
00821925038622
Version / Model
RKA-4
Company Name
Gyrus ACMI, LLC
Labeler DUNS
007198742
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-17
Public Version
3
Public Version Date
2025-01-20
Public Version Status
Update
Public Device Record Key
294e2089-1cd4-4610-8cbe-15b0d227ecd8

Device Description

Replacement Knob Assembly (4/PK)

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
No
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FAS Electrode, Electrosurgical, Active, Urological

GMDN Terms

Code Name
44776 Electrosurgical system

Identifiers

Type ID
Primary 00821925038622
Package 00821925007932

Premarket Submissions

Submission Number Supplement Number
K890328 000