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F88

FDA UDI

Class II (US FDA UDI)

by Sg Endoscopy Pte, Ltd.

Identity

Trade Name
F88 FDA UDI
Generic Name
Flexible video ureteroscope, reusable FDA UDI
Device Name
Flexible Ureteroscope, Reverse Deflection FDA UDI
Model / Reference
0502388110 FDA UDI
Description
Flexible Ureteroscope, Reverse Deflection FDA UDI

Identifiers

Catalog Number
0502388110 FDA UDI
Primary DI / UDI-DI
08881300750091 FDA UDI
510(k) Number
K243894 FDA UDI
FDA Product Code
FGB FDA UDI
GMDN Term
Flexible video ureteroscope, reusable 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Hydrogen Peroxide FDA UDI

Category: Flexible video ureteroscope, reusable

F88 by Sg Endoscopy Pte, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Flexible video ureteroscope, reusable.

Cleared under the same submission

K243894 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sg Endoscopy Pte, Ltd.

Sources (1)

  • FDA UDI 42a7f96f-03ef-4cc3-b9c4-dc18412b6e1e 36 fields · synced May 30, 2026