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Fine End (Purple) 18G / 1.0mm

FDA UDI

Class II (US FDA UDI)

by Dtr Medical Limited

Identity

Trade Name
Fine End (Purple) 18G / 1.0mm FDA UDI
Generic Name
Surgical/emergency suction cannula, non-illuminating, single-use FDA UDI
Model / Reference
74-2020 FDA UDI

Identifiers

Primary DI / UDI-DI
05060411982307 FDA UDI
FDA Product Code
JOL FDA UDI
GMDN Term
Surgical/emergency suction cannula, non-illuminating, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical/emergency suction cannula, non-illuminating, single-use

Fine End (Purple) 18G / 1.0mm by Dtr Medical Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/emergency suction cannula, non-illuminating, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dtr Medical Limited

Sources (1)

  • FDA UDI 8492d87c-3bb8-485b-bbd9-11196d996432 32 fields · synced Jun 1, 2026