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Seplou

FDA UDI

Class II (US FDA UDI)

by Seplou (Zhuhai) Co., Ltd.

Identity

Trade Name
SEPLOU FDA UDI
Generic Name
Endoscopic video image processing unit FDA UDI
Device Name
The image processor is used with the specified endoscope designed by SEPLOU during minimally invasive surgery. FDA UDI
Model / Reference
DIS8000 FDA UDI
Description
The image processor is used with the specified endoscope designed by SEPLOU during minimally invasive surgery. FDA UDI

Identifiers

Primary DI / UDI-DI
06976358503866 FDA UDI
510(k) Number
K250049 FDA UDI
FDA Product Code
FGB FDA UDI
GMDN Term
Endoscopic video image processing unit 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopic video image processing unit

Seplou by Seplou (Zhuhai) Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic video image processing unit.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 37c3b007-c756-442b-ba9a-fb18d0bc38ce 34 fields · synced Jun 1, 2026