Double Threaded Hub

FDA UDI

Class I (US FDA UDI)

by W.H. Holden, Inc.

Identity

Trade Name: DOUBLE THREADED HUB FDA UDI
Generic Name: Dental anaesthesia syringe, intraligamentary FDA UDI
Model / Reference: 10-7145-1 FDA UDI

Identifiers

Primary DI / UDI-DI: D92810714510 FDA UDI
FDA Product Code: GDM FDA UDI
GMDN Term: Dental anaesthesia syringe, intraligamentary FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Dental anaesthesia syringe, intraligamentary

Double Threaded Hub by W.H. Holden, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Dental anaesthesia syringe, intraligamentary.

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PAROJECT — Rønvig Dental Manufacturing A/S · Class II
SYRINGE-SELF-ASPIRATING — W.H. Holden, Inc. · Class I
ASPIRATING SYRINGE ASTRA TYPE — W.H. Holden, Inc. · Class I
SYRINGE-2CC-LUER-METAL HUB — W.H. Holden, Inc. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: W.H. Holden, Inc.

Sources (1)

FDA UDI 90737f25-fb4f-499a-88e4-1205cca8b633 32 fields · synced Jun 8, 2026