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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
General-purpose syringe/needle FDA UDI
Model / Reference
PCS3181K01 FDA UDI

Identifiers

Primary DI / UDI-DI
00860010450178 FDA UDI
FDA Product Code
FMF FDA UDI
GMDN Term
General-purpose syringe/needle FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5860 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: General-purpose syringe/needle

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 General-purpose syringe/needle.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 19fe8373-b64e-4536-a3fa-ffc15f1431e8 32 fields · synced Jun 8, 2026