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Adapter-H

FDA UDI

Class I (US FDA UDI)

by MCT Bio

Identity

Trade Name
Adapter-H FDA UDI
Generic Name
Dental power tool handpiece motorless component FDA UDI
Device Name
Adapter-H IMPLANT-RESCUE-ADAPT Adapter for hand BONE-EXPAND-HP-ADAPT FDA UDI
Model / Reference
Adapter-H FDA UDI
Description
Adapter-H IMPLANT-RESCUE-ADAPT Adapter for hand BONE-EXPAND-HP-ADAPT FDA UDI

Identifiers

Catalog Number
Adapter-H FDA UDI
Primary DI / UDI-DI
08800021123175 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental power tool handpiece motorless component FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 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

No

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

Category: Dental power tool handpiece motorless component

Adapter-H by MCT Bio — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental power tool handpiece motorless component.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
MCT Bio

Sources (1)

  • FDA UDI fba07384-b9ee-4aa4-919f-80181c04c397 34 fields · synced Jun 7, 2026