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Azur Medical Company Inc.

FDA UDI

Class II (US FDA UDI)

by Azur Medical Company, Inc.

Identity

Trade Name
Azur Medical Company Inc. FDA UDI
Generic Name
Medication transfer needle, non-filtering/non-vented FDA UDI
Model / Reference
CSB181H01 FDA UDI

Identifiers

Primary DI / UDI-DI
00860010450116 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
Medication transfer needle, non-filtering/non-vented FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Medication transfer needle, non-filtering/non-vented

Azur Medical Company Inc. by Azur Medical Company, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medication transfer needle, non-filtering/non-vented.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Azur Medical Company, Inc.

Sources (1)

  • FDA UDI 49713d3c-4d10-4a86-9fa4-70195948a805 32 fields · synced Jun 6, 2026