FDA UDI In Commercial Distribution 🇺🇸 United States

Curette

DI: 10840199522245 · Model: 7391-92F · KOROS U.S.A., INC.
Product Codes
1
GMDN Terms
3
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Curette
Primary DI
10840199522245
Version / Model
7391-92F
Catalog Number
7391-92F
Company Name
KOROS U.S.A., INC.
Labeler DUNS
007928633
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-01
Public Version
1
Public Version Date
2021-12-09
Public Version Status
New
Public Device Record Key
dce29382-1914-475b-9e49-80fc5b05b743

Device Description

Lateral Curette Epstein Down-Pusher Tip with Offset Handle, Size 3, 8-1/2" Shaft 21.5cm, 9-3/4" 25cm Handle, Total Length 18-1/4" 46.5cm

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
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
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
62558 General-purpose curette
31335 Bone curette, reusable
32772 Ophthalmic curette, reusable

Identifiers

Type ID
Direct Marking 00840199522248
Primary 10840199522245

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 3mm tip

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in dry place at room temperature