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Shifeng

FDA UDI

Class I (US FDA UDI)

by Shifeng Medical Technology Co.,ltd.

Identity

Trade Name
Shifeng FDA UDI
Generic Name
Luer-formatted protective cap FDA UDI
Model / Reference
UU118 FDA UDI

Identifiers

Primary DI / UDI-DI
G002UU1180 FDA UDI
FDA Product Code
KDC FDA UDI
GMDN Term
Luer-formatted protective cap FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Category: Luer-formatted protective cap

Shifeng by Shifeng Medical Technology Co.,ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luer-formatted protective cap.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 72e4f8c0-1ea4-41e5-815c-920dad97283b 32 fields · synced May 30, 2026