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Kiato

FDA UDI

Class I (US FDA UDI)

by Aditya Dispomed Products Private Limited

Identity

Trade Name
KIATO FDA UDI
Generic Name
Manual scalpel blade, single-use FDA UDI
Device Name
KIATO Sterile CE carbon Steel Surgical Blade Box of 100 size 11P. Sterilized by Gamma Irradiation. FDA UDI
Model / Reference
11P FDA UDI
Description
KIATO Sterile CE carbon Steel Surgical Blade Box of 100 size 11P. Sterilized by Gamma Irradiation. FDA UDI

Identifiers

Catalog Number
11161 FDA UDI
Primary DI / UDI-DI
08902895111613 FDA UDI
FDA Product Code
GES FDA UDI
GMDN Term
Manual scalpel blade, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Manual scalpel blade, single-use

Kiato by Aditya Dispomed Products Private Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual scalpel blade, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0e7863b2-59fa-402d-8be1-0bf85d5aa3c8 35 fields · synced May 30, 2026