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Medlot

FDA UDI

Class I (US FDA UDI)

by Henan Maidingkang Medical Technology Co., Ltd.

Identity

Trade Name
MEDLOT FDA UDI
Generic Name
Scar-management dressing, reusable FDA UDI
Model / Reference
10*18cm FDA UDI

Identifiers

Primary DI / UDI-DI
06974795054538 FDA UDI
FDA Product Code
PFP FDA UDI
GMDN Term
Scar-management dressing, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4025 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

Yes

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: Scar-management dressing, reusable

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

Similar devices

Also classified as Scar-management dressing, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4db72958-314a-4d51-a3fb-643d85611772 32 fields · synced May 31, 2026