Tech Medical Service

FDA UDI

Class II (US FDA UDI)

by Tech Medical Services, Inc.

Identity

Trade Name: Tech Medical Service FDA UDI
Generic Name: General-purpose endoscopic needle, single-use FDA UDI
Device Name: Veress Needle FDA UDI
Model / Reference: IN-15-24 FDA UDI
Description: Veress Needle FDA UDI

Identifiers

Primary DI / UDI-DI: 00851695005647 FDA UDI
510(k) Number: K111441 FDA UDI
FDA Product Code: HIF FDA UDI
GMDN Term: General-purpose endoscopic needle, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 884.1730 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Ethylene Oxide FDA UDI

Category: General-purpose endoscopic needle, single-use

Tech Medical Service by Tech Medical Services, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose endoscopic needle, single-use.

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Injectra, ScleroTip — Medi-Globe Corporation · Class II
Single Use Injector NM600/610 — Olympus Medical Systems Corporation · Class II
Single Use Aspiration Needle NA-U401SX — Olympus Medical Systems Corporation · Class II
Henry Schein — HENRY SCHEIN, INC. · Class I

Cleared under the same submission

K111441 also covers:

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 II	Pending data

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Manufacturer

Manufacturer: Tech Medical Services, Inc.

Sources (1)

FDA UDI 1f59e882-24e6-4981-bb45-2c48f451bf8b 34 fields · synced Jun 6, 2026