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Henry Schein

FDA UDI

Class I (US FDA UDI)

by Henry Schein, Inc.

Identity

Trade Name
Henry Schein FDA UDI
Generic Name
Anaesthesia Luer syringe, non-sterile FDA UDI
Device Name
Dental syringe, 6cc Luer Lock Non sterile FDA UDI
Model / Reference
5701403 FDA UDI
Description
Dental syringe, 6cc Luer Lock Non sterile FDA UDI

Identifiers

Catalog Number
5701403 FDA UDI
Primary DI / UDI-DI
10304040108786 FDA UDI
FDA Product Code
EIC FDA UDI
GMDN Term
Anaesthesia Luer syringe, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

No

FDA UDI

Over-the-Counter

Yes

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Anaesthesia Luer syringe, non-sterile

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

Similar devices

Also classified as Anaesthesia Luer syringe, non-sterile.

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 3e0fbc4b-5a77-4bd4-a39a-2eb483f13f0a 34 fields · synced Jun 8, 2026