← Back to catalogue

Hahn

FDA UDI

Class I (US FDA UDI)

by Prismatik Dentalcraft, Inc.

Identity

Trade Name
Hahn FDA UDI
Generic Name
Dental torque wrench adaptor FDA UDI
Device Name
Hahn Tapered Implant Surgical Adaptor - Short FDA UDI
Model / Reference
70-1071-SRG0231 FDA UDI
Description
Hahn Tapered Implant Surgical Adaptor - Short FDA UDI

Identifiers

Catalog Number
70-1071-SRG0231 FDA UDI
Primary DI / UDI-DI
D745701071SRG02310 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental torque wrench adaptor 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental torque wrench adaptor

Hahn by Prismatik Dentalcraft, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental torque wrench adaptor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI e6d87c52-2a5f-493f-b7d9-437ada5adac0 35 fields · synced Jun 1, 2026