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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
Root canal irrigation blunt needle FDA UDI
Device Name
Irrigating Needles Side Vent FDA UDI
Model / Reference
1025272 FDA UDI
Description
Irrigating Needles Side Vent FDA UDI

Identifiers

Catalog Number
1025272 FDA UDI
Primary DI / UDI-DI
10304040058852 FDA UDI
FDA Product Code
DZM FDA UDI
GMDN Term
Root canal irrigation blunt needle FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4730 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Root canal irrigation blunt needle

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

Similar devices

Also classified as Root canal irrigation blunt needle.

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 dd738d1d-9f3a-4d2d-8491-018302a1590d 34 fields · synced Jun 6, 2026