← Back to catalogue

Vectortas Crimpable Post Pk6

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 601-0040

by Ormco Corporation

Identity

Trade Name
VECTORTAS CRIMPABLE POST PK6 EUDAMED
VECTOR TAS FDA UDI
Generic Name
Orthodontic anchoring screw FDA UDI
Device Name
VECTORTAS CRIMPABLE POST PK6 EUDAMED
VECTOR TAS CRIMPABLE POST Qty 6 FDA UDI
Model / Reference
601-0040 EUDAMEDFDA UDI
Description
VECTOR TAS CRIMPABLE POST Qty 6 FDA UDI

Identifiers

Primary DI / UDI-DI
00889989000214 EUDAMED
10889989000211 FDA UDI
Basic UDI-DI
0889989-VTAS_CrimpPost-DV EUDAMED
FDA Product Code
OAT FDA UDI
EMDN Code
P01020180 DENTAL IMPLANTS - ACCESSORIES EUDAMED
GMDN Term
Orthodontic anchoring screw FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
872.3640 FDA UDI
Market of Registration
Italy EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

The VECTORTAS CRIMPABLE POST PK6 medical device is a Class IIa instrument used for endodontic procedures. It features a crispable post and is designed to provide precise control over the treatment process. The device has undergone rigorous testing and evaluation, ensuring its safety and efficacy in clinical settings.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Ormco Corporation
EUDAMED SRN
US-MF-000038085
Authorised Representative
KERR ITALIA SRL IT-AR-000007600

Sources (2)

  • EUDAMED 1a924578-5949-4d9b-a8af-ef303a9733ef 61 fields · synced Jul 25, 2026
  • FDA UDI ac421e08-280b-4e6f-98e1-b7d84c85417b 34 fields · synced May 30, 2026