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Hayden Medical

FDA UDI

Class I (US FDA UDI)

by Hayden Medical Inc

Identity

Trade Name
Hayden Medical FDA UDI
Generic Name
Body aspiration needle, reusable FDA UDI
Device Name
Transfer hub, female luer ends, ID 1.2mm FDA UDI
Model / Reference
NFT-1.2 FDA UDI
Description
Transfer hub, female luer ends, ID 1.2mm FDA UDI

Identifiers

Catalog Number
NFT-1.2 FDA UDI
Primary DI / UDI-DI
00840319752685 FDA UDI
FDA Product Code
GDM FDA UDI
GMDN Term
Body aspiration needle, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Body aspiration needle, reusable

Hayden Medical by Hayden Medical Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Body aspiration needle, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hayden Medical Inc

Sources (1)

  • FDA UDI e195c0b7-9586-4154-a11e-f558401b8d0a 35 fields · synced Jun 1, 2026