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Hupai

FDA UDI

Class I (US FDA UDI)

by Jiangsu Chongheng Medical Technology Co., Ltd.

Identity

Trade Name
Hupai FDA UDI
Generic Name
Blood collection set, invasive FDA UDI
Model / Reference
3ml 0.7×30mm FDA UDI

Identifiers

Primary DI / UDI-DI
06976025820012 FDA UDI
FDA Product Code
CBT FDA UDI
GMDN Term
Blood collection set, invasive FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.1100 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Blood collection set, invasive

Hupai by Jiangsu Chongheng Medical Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood collection set, invasive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4d021162-604f-4f00-b167-973856ef370c 32 fields · synced Jun 1, 2026