Baixin

FDA UDI

Class II (US FDA UDI)

by Anhui Kangda Medical Products Co., Ltd.

Identity

Trade Name: BAIXIN FDA UDI
Generic Name: Basic intravenous administration set, invasive FDA UDI
Model / Reference: KD210 FDA UDI

Identifiers

Primary DI / UDI-DI: 06936018501014 FDA UDI
FDA Product Code: FPA FDA UDI
GMDN Term: Basic intravenous administration set, invasive FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5440 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

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: Basic intravenous administration set, invasive

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

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SURFLO — Terumo Medical Products (Hangzhou) Co., Ltd. · Class II
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VACUETTE — Greiner Bio-One GmbH · Class II
ULTRAFLO-R — Innovative Medical Technologies, Inc. · Class II

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 II	Pending data

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Manufacturer

Manufacturer: Anhui Kangda Medical Products Co., Ltd.

Sources (1)

FDA UDI 027d5867-c683-473e-afef-78658fdf712b 32 fields · synced Jun 8, 2026