Identity

Trade Name
Lorski FDA UDI
Generic Name
Scar-management dressing, single-use FDA UDI
Device Name
lintended Usel:It is used to assist in imnroving skin Pathological scars and assist in preventing the formation of skin pathological scars, not for unhealed wounds. FDA UDI
Model / Reference
3×5cm FDA UDI
Description
lintended Usel:It is used to assist in imnroving skin Pathological scars and assist in preventing the formation of skin pathological scars, not for unhealed wounds. FDA UDI

Identifiers

Primary DI / UDI-DI
06941917833173 FDA UDI
FDA Product Code
MDA FDA UDI
GMDN Term
Scar-management dressing, single-use 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

No

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, single-use

Lorski by Shandong Zhushi Pharmaceutical Group Co., Ltd. First Office — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Scar-management dressing, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 80e54db8-caa5-47f3-a83b-0e2989d1b0da 33 fields · synced Jun 8, 2026