FDA UDI In Commercial Distribution 🇺🇸 United States

Kevorkian Curette

DI: 00888937017359 · Model: 66-440 · Coopersurgical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kevorkian Curette
Primary DI
00888937017359
Version / Model
66-440
Company Name
Coopersurgical, Inc.
Labeler DUNS
801895244
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-08
Public Version
3
Public Version Date
2024-02-28
Public Version Status
Update
Public Device Record Key
2f2cc109-e872-474a-8edb-262570a564e5

Device Description

Kevorkian Curette without basket

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
FZS Curette, Surgical, General Use

GMDN Terms

Code Name
46871 Endometrial biopsy curette

Identifiers

Type ID
Primary 00888937017359

Device Sizes

Type Value Unit Text
Length 305 Millimeter