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Osung Mnd

FDA UDI

Class II (US FDA UDI)

by Osung Mnd Co., Ltd.

Identity

Trade Name
OSUNG MND FDA UDI
Generic Name
Dental impression material syringe, reusable FDA UDI
Device Name
A non-sterile, hand-held manual dental instrument consisting of a barrel (cylinder) with plunger intended to be used to inject impression material into an impression tray or directly into a patient's mouth. This is a reusable device. FDA UDI
Model / Reference
SBA18T3 FDA UDI
Description
A non-sterile, hand-held manual dental instrument consisting of a barrel (cylinder) with plunger intended to be used to inject impression material into an impression tray or directly into a patient's mouth. This is a reusable device. FDA UDI

Identifiers

Primary DI / UDI-DI
08800075626356 FDA UDI
FDA Product Code
EJI FDA UDI
GMDN Term
Dental impression material syringe, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.6770 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental impression material syringe, reusable

Osung Mnd by Osung Mnd Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental impression material syringe, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Osung Mnd Co., Ltd.

Sources (1)

  • FDA UDI 7f9fd362-6b3e-4b46-b147-2c2d21a5cdaf 33 fields · synced May 30, 2026