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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
Dental material injection cannula, reusable FDA UDI
Device Name
Retreat GRP Cannules FDA UDI
Model / Reference
5700346 FDA UDI
Description
Retreat GRP Cannules FDA UDI

Identifiers

Catalog Number
5700346 FDA UDI
Primary DI / UDI-DI
10304040025984 FDA UDI
510(k) Number
K050180 FDA UDI
FDA Product Code
MVL FDA UDI
GMDN Term
Dental material injection cannula, reusable FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental material injection cannula, reusable

Henry Schein by Henry Schein, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental material injection cannula, reusable.

Cleared under the same submission

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 607ced8a-6f1f-4eb7-88fa-5be541ad67cf 35 fields · synced Jun 8, 2026