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Robbins Dermo-jet

FDA UDI

Class II (US FDA UDI)

by Robbins Instruments

Identity

Trade Name
Robbins Dermo-jet FDA UDI
Generic Name
Needleless medication/vaccine injector, mechanical FDA UDI
Device Name
The Original Needle-Free Injection Device FDA UDI
Model / Reference
DJ-05 FDA UDI
Description
The Original Needle-Free Injection Device FDA UDI

Identifiers

Catalog Number
DJ-05 FDA UDI
Primary DI / UDI-DI
00199284222250 FDA UDI
FDA Product Code
KZE FDA UDI
GMDN Term
Needleless medication/vaccine injector, mechanical FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5430 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

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Needleless medication/vaccine injector, mechanical

Robbins Dermo-jet by Robbins Instruments — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Needleless medication/vaccine injector, mechanical.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Robbins Instruments

Sources (1)

  • FDA UDI 371e8ef1-8c1c-4e97-835f-e5e5f645fb87 35 fields · synced Jun 8, 2026