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AladuckII V100

FDA UDI

Class II (US FDA UDI)

by Sbi Pharmaceuticals Co., Ltd.

Identity

Trade Name
AladuckII V100 FDA UDI
Generic Name
Endoscopic light source unit, line-powered FDA UDI
Device Name
AladuckII V100 FDA UDI
Model / Reference
220-23 FDA UDI
Description
AladuckII V100 FDA UDI

Identifiers

Catalog Number
220-23 FDA UDI
Primary DI / UDI-DI
04560304635743 FDA UDI
FDA Product Code
NTN FDA UDI
GMDN Term
Endoscopic light source unit, line-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopic light source unit, line-powered

AladuckII V100 by Sbi Pharmaceuticals Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic light source unit, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 34228f5c-f140-4652-bbde-c0e35392c391 34 fields · synced May 30, 2026