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Kamiyama

FDA UDI

Class I (US FDA UDI)

by Takayama Instruments Inc.

Identity

Trade Name
Kamiyama FDA UDI
Generic Name
Craniofacial rongeur, reusable FDA UDI
Device Name
Micro Rongeur K-Bayonet, 200mm (90mm W.L.), Slightly Curved Tip FDA UDI
Model / Reference
KT-702 FDA UDI
Description
Micro Rongeur K-Bayonet, 200mm (90mm W.L.), Slightly Curved Tip FDA UDI

Identifiers

Catalog Number
KT-702 FDA UDI
Primary DI / UDI-DI
04580036673189 FDA UDI
FDA Product Code
HTX FDA UDI
GZX FDA UDI
GMDN Term
Craniofacial rongeur, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
882.4525 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Craniofacial rongeur, reusable

Kamiyama by Takayama Instruments Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Craniofacial rongeur, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI fe59cd51-eec5-48ff-80f6-39021e2d4e6f 34 fields · synced May 30, 2026