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Medetz Surgical Instruments

FDA UDI

Class I (US FDA UDI)

by Medetz Surgical Instruments

Identity

Trade Name
Medetz Surgical Instruments FDA UDI
Generic Name
General-purpose endoscopic needle, reusable FDA UDI
Device Name
Septum Needle, 22g TW 0.8mm, OL129mm (5 1/8") FDA UDI
Model / Reference
13-1806 FDA UDI
Description
Septum Needle, 22g TW 0.8mm, OL129mm (5 1/8") FDA UDI

Identifiers

Primary DI / UDI-DI
G2231318060 FDA UDI
FDA Product Code
LRC FDA UDI
GMDN Term
General-purpose endoscopic needle, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: General-purpose endoscopic needle, reusable

Medetz Surgical Instruments by Medetz Surgical Instruments — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose endoscopic needle, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medetz Surgical Instruments

Sources (1)

  • FDA UDI eee54a94-c4e9-474e-8c04-c58b3e144123 34 fields · synced Jun 1, 2026