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Emsrun

FDA UDI

Class I (US FDA UDI)

by Wuxi Emsrun Technology Co., Ltd.

Identity

Trade Name
EMSRUN FDA UDI
Generic Name
Secretion/excreta skin cleanser FDA UDI
Model / Reference
PZFZ0001 FDA UDI

Identifiers

Primary DI / UDI-DI
06974567741123 FDA UDI
FDA Product Code
LRJ FDA UDI
GMDN Term
Secretion/excreta skin cleanser FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6890 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
High Intensity Light or Pulse Light FDA UDI

Category: Secretion/excreta skin cleanser

Emsrun by Wuxi Emsrun Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Secretion/excreta skin cleanser.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI eed8b3e8-f028-4769-976b-3bb954841761 32 fields · synced May 31, 2026