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SilTrax AS Retraction Cord 7/00

FDA UDI

Class U (US FDA UDI)

by Pascal Company, Inc.

Identity

Trade Name
SilTrax AS Retraction Cord 7/00 FDA UDI
Generic Name
Gingival retraction cord, non-medicated FDA UDI
Device Name
Braided Gingival Retraction Cord with Aluminum Sulfate, 72 inches, Size 7/00 FDA UDI
Model / Reference
07097 FDA UDI
Description
Braided Gingival Retraction Cord with Aluminum Sulfate, 72 inches, Size 7/00 FDA UDI

Identifiers

Catalog Number
07097 FDA UDI
Primary DI / UDI-DI
00310866000329 FDA UDI
FDA Product Code
MVL FDA UDI
GMDN Term
Gingival retraction cord, non-medicated FDA UDI

Classification

Device Class
U 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

Yes

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

SilTrax AS Retraction Cord 7/00 by Pascal Company, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gingival retraction cord, non-medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 02973b3d-0330-46d5-830d-6829c2b65b90 36 fields · synced Jun 6, 2026