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Amniocentesis Tray

FDA UDI

Class I (US FDA UDI)

by Argon Medical Devices, Inc.

Identity

Trade Name
Amniocentesis Tray FDA UDI
Generic Name
Amniocentesis kit, medicated, single-use FDA UDI
Device Name
Amniocentesis Tray with 20ga x 8.9cm Needle FDA UDI
Model / Reference
A4545A FDA UDI
Description
Amniocentesis Tray with 20ga x 8.9cm Needle FDA UDI

Identifiers

Catalog Number
A4545A FDA UDI
Primary DI / UDI-DI
00886333220793 FDA UDI
FDA Product Code
HIO FDA UDI
GMDN Term
Amniocentesis kit, medicated, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.1550 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Amniocentesis Tray by Argon Medical Devices, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 269337c8-b70e-43ef-8dc1-40992d0551bb 37 fields · synced Jun 9, 2026