← Back to catalogue

Pt-55

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 26135

by Pascal Company Inc.

Identity

Trade Name
PT-55 EUDAMED
PT-55 Packing Instrument FDA UDI
Generic Name
Gingival retraction cord packing tool FDA UDI
Device Name
Packing Instruments EUDAMED
Retraction Cord Packing Instrument, Circlet instrument with serrated tip FDA UDI
Model / Reference
26135 EUDAMEDFDA UDI
Description
Retraction Cord Packing Instrument, Circlet instrument with serrated tip FDA UDI

Identifiers

Catalog Number
26135 FDA UDI
Primary DI / UDI-DI
00310866000718 EUDAMEDFDA UDI
Basic UDI-DI
03108669001HF EUDAMED
FDA Product Code
EIF FDA UDI
EMDN Code
Q010204 RETRACTION WIRES AND GINGIVAL RETRACTORS EUDAMED
GMDN Term
Gingival retraction cord packing tool FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.4565 FDA UDI
Market of Registration
Croatia 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

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

Category: Gingival retraction cord, non-medicated

Pt-55 by Pascal Company, Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gingival retraction cord, non-medicated.

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
Pascal Company Inc.
EUDAMED SRN
US-MF-000032036
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED f84c78f3-0add-4fa2-a534-540957caeda3 61 fields · synced Jul 25, 2026
  • FDA UDI 5ae620e1-817f-4da9-a1d8-cc051ed1be5a 35 fields · synced May 30, 2026