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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
Open surgical site internal light FDA UDI
Model / Reference
PZBB0005-2 FDA UDI

Identifiers

Primary DI / UDI-DI
06974567743325 FDA UDI
FDA Product Code
KYT FDA UDI
GMDN Term
Open surgical site internal light FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6350 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

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: Open surgical site internal light

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

Similar devices

Also classified as Open surgical site internal light.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5e153988-8142-47db-8c7c-e4a0f7f36cdc 32 fields · synced May 30, 2026