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Henry Schein

FDA UDI

Class U (US FDA UDI)

by Henry Schein, Inc.

Identity

Trade Name
Henry Schein FDA UDI
Generic Name
Gingival retraction cord, non-medicated FDA UDI
Device Name
Retreat w/Aluminum Sulfate FDA UDI
Model / Reference
1008490 FDA UDI
Description
Retreat w/Aluminum Sulfate FDA UDI

Identifiers

Catalog Number
1008490 FDA UDI
Primary DI / UDI-DI
00304040015490 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

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

Yes

FDA UDI

Category: Gingival retraction cord, non-medicated

Henry Schein by Henry Schein, 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

Manufacturer
Henry Schein, Inc.

Sources (1)

  • FDA UDI 6076ced8-3013-4aed-8ca8-283aa9a1034b 34 fields · synced May 30, 2026