FDA UDI In Commercial Distribution 🇺🇸 United States

Kerrison Rongeur

DI: 10840199520395 · Model: 7380-79 · KOROS U.S.A., INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Kerrison Rongeur
Primary DI
10840199520395
Version / Model
7380-79
Catalog Number
7380-79
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
2024-05-31
Public Version
1
Public Version Date
2024-06-10
Public Version Status
New
Public Device Record Key
2383d8a5-1b54-4aff-b868-d2e26834ed7e

Device Description

Kerrison Rongeur Large Handle 4mm x 40 deg

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
HTX Rongeur

GMDN Terms

Code Name
32853 Orthopaedic joint/limb rongeur

Identifiers

Type ID
Direct Marking 00840199520398
Primary 10840199520395

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