FDA UDI In Commercial Distribution 🇺🇸 United States

GYRUS ACMI

DI: 00821925033382 · Model: 130761 · Gyrus Acmi, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
GYRUS ACMI
Primary DI
00821925033382
Version / Model
130761
Company Name
Gyrus Acmi, Inc.
Labeler DUNS
007198742
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-10
Public Version
3
Public Version Date
2023-08-25
Public Version Status
Update
Public Device Record Key
0ec2c0b7-9686-4e03-a440-9f5c3f7b5576

Device Description

BUCK WAX CURETTE DISPOSABLE SIZE 2

Device Characteristics

Single Use
Yes
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LRC INSTRUMENT, ENT MANUAL SURGICAL

GMDN Terms

Code Name
62558 General-purpose curette

Identifiers

Type ID
Package 00821925017788
Primary 00821925033382