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MD Resource

FDA UDI

Class I (US FDA UDI)

by Medical Device Resource Corp.

Identity

Trade Name
MD Resource FDA UDI
Generic Name
Dual spike connector FDA UDI
Device Name
AutoFuse Tubing Disposable, Y-Connection FDA UDI
Model / Reference
AFTD-Y FDA UDI
Description
AutoFuse Tubing Disposable, Y-Connection FDA UDI

Identifiers

Catalog Number
AFTD-Y FDA UDI
Primary DI / UDI-DI
00859898006065 FDA UDI
FDA Product Code
KGZ FDA UDI
GMDN Term
Dual spike connector FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dual spike connector

MD Resource by Medical Device Resource Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dual spike connector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0e98f9dc-db1d-4f26-aadd-f443aeea60cd 34 fields · synced May 30, 2026