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Expansion tool-screw 6.35+wrench short - Assy

FDA UDI

Class I (US FDA UDI)

by Dentack Implants Ltd

Identity

Trade Name
Expansion tool-screw 6.35+wrench short - Assy FDA UDI
Generic Name
Dental torque wrench FDA UDI
Device Name
Expansion tool-screw 6.35+wrench short - Assy FDA UDI
Model / Reference
ET-1850 FDA UDI
Description
Expansion tool-screw 6.35+wrench short - Assy FDA UDI

Identifiers

Primary DI / UDI-DI
07290112280831 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental torque wrench FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Expansion tool-screw 6.35+wrench short - Assy by Dentack Implants Ltd — 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 d9eb8632-c1d6-41a0-9f1c-9a22c1c95596 35 fields · synced Jun 6, 2026