Pre-Bent Flow Tips

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name: Pre-Bent Flow Tips FDA UDI
Generic Name: Dental anaesthesia syringe/needle FDA UDI
Device Name: Pre-Bent Flow Tips, 25g, Etch Tips, Blue FDA UDI
Model / Reference: 2213 FDA UDI
Description: Pre-Bent Flow Tips, 25g, Etch Tips, Blue FDA UDI

Identifiers

Primary DI / UDI-DI: 00616784221311 FDA UDI
FDA Product Code: DZM FDA UDI
GMDN Term: Dental anaesthesia syringe/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

FDA UDI

Single Use

Yes

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

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Dental anaesthesia syringe/needle

Pre-Bent Flow Tips by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental anaesthesia syringe/needle.

MAX-JECT DENTAL NEEDLES — MAXILL, INC. · Class I
MAX-JECT DENTAL NEEDLES — MAXILL, INC. · Class I
MAX-JECT DENTAL NEEDLES — MAXILL, INC. · Class I
MAX-JECT DENTAL NEEDLES — MAXILL, INC. · Class I
MAX-JECT DENTAL NEEDLES — MAXILL, INC. · Class I
MAX-JECT DENTAL NEEDLES — MAXILL, INC. · Class I
MAX-JECT DENTAL NEEDLES — MAXILL, INC. · Class I
Pre-Bent Flow Tips — Dynarex Corp. · 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: Dynarex Corp.

Sources (1)

FDA UDI 3436d4e4-13f7-4b3e-b211-2303cf7a317c 33 fields · synced May 30, 2026