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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, 18G, Pink, 100/bag, 25/bag, CS FDA UDI
Model / Reference
2211 FDA UDI
Description
Pre-Bent Flow Tips, 18G, Pink, 100/bag, 25/bag, CS FDA UDI

Identifiers

Primary DI / UDI-DI
00616784221113 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

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

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

No

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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI d09b91e1-a59c-4e9a-895e-e01dc067526c 33 fields · synced May 30, 2026