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Intradermal Cannulae

FDA UDI

Class II (US FDA UDI)

by Sterimedix Limited

Identity

Trade Name
Intradermal Cannulae FDA UDI
Generic Name
Tissue injection cannula FDA UDI
Device Name
Silkann(FT)Cann 18gx70mm FDA UDI
Model / Reference
AJ1701-02/40 FDA UDI
Description
Silkann(FT)Cann 18gx70mm FDA UDI

Identifiers

Catalog Number
AJ1701 FDA UDI
Primary DI / UDI-DI
25056030402658 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

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
Sterilization Method
Ethylene Oxide FDA UDI

Category: Tissue injection cannula

Intradermal Cannulae by Sterimedix Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Tissue injection cannula.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sterimedix Limited

Sources (1)

  • FDA UDI 129174fd-4d60-4d12-ac43-562b5d51359f 34 fields · synced Jun 1, 2026