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DS PrimeTaper

FDA UDI

Class I (US FDA UDI)

by Dentsply Implants Manufacturing GmbH

Identity

Trade Name
DS PrimeTaper FDA UDI
Generic Name
Surgical drill guide, single-use FDA UDI
Device Name
PrimeTaper Drill Sleeve 1 WD GS FDA UDI
Model / Reference
68017291 FDA UDI
Description
PrimeTaper Drill Sleeve 1 WD GS FDA UDI

Identifiers

Catalog Number
68017291 FDA UDI
Primary DI / UDI-DI
07392532279645 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Surgical drill guide, single-use 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

Yes

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

No

FDA UDI

Category: Surgical drill guide, single-use

DS PrimeTaper by Dentsply Implants Manufacturing GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical drill guide, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 546862c0-a6b0-4187-b4ed-da8f3e460108 34 fields · synced May 30, 2026