Intradermal Cannulae and Needles

FDA UDI

Class II (US FDA UDI)

by Sterimedix Limited

Identity

Trade Name: Intradermal Cannulae and Needles FDA UDI
Generic Name: Tissue injection cannula FDA UDI
Device Name: Silkann(FT) Cann 22gx60mm FDA UDI
Model / Reference: AJ1832A-02/25 FDA UDI
Description: Silkann(FT) Cann 22gx60mm FDA UDI

Identifiers

Catalog Number: AJ1832A FDA UDI
Primary DI / UDI-DI: 15056030402675 FDA UDI
FDA Product Code: MED FDA UDI
GMDN Term: Tissue injection cannula FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.6885 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

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Ethylene Oxide FDA UDI

Category: Tissue injection cannula

Intradermal Cannulae and Needles by Sterimedix Limited — 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: Sterimedix Limited

Sources (1)

FDA UDI 40799c3e-5fed-4346-bd85-2ab5f888d4d2 34 fields · synced Jun 1, 2026