Baixin

FDA UDI

Class I (US FDA UDI)

by Anhui Kangda Medical Products Co., Ltd.

Identity

Trade Name: BAIXIN FDA UDI
Generic Name: Blood collection set, invasive FDA UDI
Model / Reference: 23GSVS FDA UDI

Identifiers

Primary DI / UDI-DI: 06936018501762 FDA UDI
FDA Product Code: GIO FDA UDI
GMDN Term: Blood collection set, invasive FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 864.6150 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Ethylene Oxide FDA UDI

Category: Blood collection set, invasive

Baixin by Anhui Kangda Medical Products Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Anhui Kangda Medical Products Co., Ltd.

Sources (1)

FDA UDI ab3a6e54-9d62-46bb-a31f-24d68dc95039 32 fields · synced May 30, 2026