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Kohdent

FDA UDI

Class I (US FDA UDI)

by Kohler Medizintechnik GmbH & Co. KG

Identity

Trade Name
KOHDENT FDA UDI
Generic Name
Needleless medication/vaccine injector, mechanical FDA UDI
Device Name
Dovgan MTA Carrier 0,99 mm FDA UDI
Model / Reference
3577 FDA UDI
Description
Dovgan MTA Carrier 0,99 mm FDA UDI

Identifiers

Catalog Number
3577 FDA UDI
Primary DI / UDI-DI
04251436932144 FDA UDI
FDA Product Code
EIC FDA UDI
GMDN Term
Needleless medication/vaccine injector, mechanical FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
Not 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

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Kohdent by Kohler Medizintechnik GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5cbcb99e-df6f-4cdb-b808-ab4544c6a133 36 fields · synced May 29, 2026