FDA UDI In Commercial Distribution 🇺🇸 United States

KW

DI: 04580036674414 · Model: KW-90MF · TAKAYAMA INSTRUMENTS INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KW
Primary DI
04580036674414
Version / Model
KW-90MF
Catalog Number
KW-90MF
Company Name
TAKAYAMA INSTRUMENTS INC.
Labeler DUNS
707948014
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-06-26
Public Version
1
Public Version Date
2025-07-04
Public Version Status
New
Public Device Record Key
9bf51ccc-4d97-4cef-a0eb-27622a08ebd1

Device Description

Membrane-Tumor-Grasping Universal forceps Bayonet, 195mm (90mm W.L.)

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
Yes
PM Exempt
Yes
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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GEN Forceps, General & Plastic Surgery

GMDN Terms

Code Name
62466 Surgical soft-tissue manipulation forceps, tweezers-like, reusable

Identifiers

Type ID
Primary 04580036674414