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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
ENT elevator FDA UDI
Device Name
Mansing Elevator, delicate, double ended, 76.2mm on both arm lengths, OL230mm (9") FDA UDI
Model / Reference
9-15980 FDA UDI
Description
Mansing Elevator, delicate, double ended, 76.2mm on both arm lengths, OL230mm (9") FDA UDI

Identifiers

Primary DI / UDI-DI
G2239159800 FDA UDI
FDA Product Code
KAD FDA UDI
GMDN Term
ENT elevator 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

Yes

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: ENT elevator

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

Similar devices

Also classified as ENT elevator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9016cc1c-7b78-4c90-8638-6dff54cdf5e1 34 fields · synced May 30, 2026