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Knittrax Plain

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 07569

by Pascal Company Inc.

Identity

Trade Name
KnitTrax Plain Retraction Cord 000 FDA UDI
Generic Name
Gingival retraction cord, non-medicated FDA UDI
Device Name
Knittrax Plain EUDAMED
Knitted Non Medicated Gingival Retraction Cord, 100 inches, Size 000 FDA UDI
Model / Reference
07569 EUDAMEDFDA UDI
Description
Knitted Non Medicated Gingival Retraction Cord, 100 inches, Size 000 FDA UDI

Identifiers

Catalog Number
07569 FDA UDI
Primary DI / UDI-DI
00310866000275 EUDAMEDFDA UDI
Basic UDI-DI
03108662003G2 EUDAMED
FDA Product Code
MVL FDA UDI
EMDN Code
Q010204 RETRACTION WIRES AND GINGIVAL RETRACTORS EUDAMED
GMDN Term
Gingival retraction cord, non-medicated FDA UDI

Classification

Device Class
Class I EUDAMED
U FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Gingival retraction cord, non-medicated

Knittrax Plain 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

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Manufacturer

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

Sources (2)

  • EUDAMED 4f75e1d6-d43b-40f9-9132-671d8c54ee26 61 fields · synced Jul 13, 2026
  • FDA UDI 8c20b944-545e-415f-9845-2464041d93a0 36 fields · synced May 30, 2026