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Mdk-Medical

FDA UDI

Class I (US FDA UDI)

by Henan Maidingkang Medical Technology Co., Ltd.

Identity

Trade Name
MDK-MEDICAL FDA UDI
Generic Name
Intestinal ostomy bag/support kit FDA UDI
Model / Reference
29*14.2cm FDA UDI

Identifiers

Primary DI / UDI-DI
06974795058581 FDA UDI
FDA Product Code
EXH FDA UDI
GMDN Term
Intestinal ostomy bag/support kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5900 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intestinal ostomy bag/support kit

Mdk-Medical by Henan Maidingkang Medical Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intestinal ostomy bag/support kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bd5820c5-7988-4835-8b86-a9d547dfef75 32 fields · synced May 30, 2026