Exel His Rotating Wing, Non-Dehp W/O Y 20gx1"

FDA UDI

Class II (US FDA UDI)

by Exel International

Identity

Trade Name: EXEL HIS ROTATING WING, NON-DEHP W/O Y 20GX1" FDA UDI
Generic Name: Subcutaneous infusion/injection port needle FDA UDI
Device Name: EXEL HIS ROTATING WING, NON-DEHP W/O Y 20GX1", 25/INNERBX, 50/BX, 20BX/CRTN FDA UDI
Model / Reference: 27954R FDA UDI
Description: EXEL HIS ROTATING WING, NON-DEHP W/O Y 20GX1", 25/INNERBX, 50/BX, 20BX/CRTN FDA UDI

Identifiers

Catalog Number: 27954R FDA UDI
Primary DI / UDI-DI: 00020221079548 FDA UDI
FDA Product Code: FPA FDA UDI
GMDN Term: Subcutaneous infusion/injection port needle FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5440 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Subcutaneous infusion/injection port needle

Exel His Rotating Wing, Non-Dehp W/O Y 20gx1" by Exel International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Exel International

Sources (1)

FDA UDI d1ea7ca2-444e-4db7-a808-3dc7d363a7ab 35 fields · synced Jun 6, 2026