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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
Adenotome FDA UDI
Device Name
Laforce Adenotome, size 1, small, BW 12.0mm, OL235mm (9 1/4") FDA UDI
Model / Reference
13-59491 FDA UDI
Description
Laforce Adenotome, size 1, small, BW 12.0mm, OL235mm (9 1/4") FDA UDI

Identifiers

Primary DI / UDI-DI
G22313594910 FDA UDI
FDA Product Code
KBH FDA UDI
GMDN Term
Adenotome 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: Adenotome

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

Similar devices

Also classified as Adenotome.

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 30c540ee-1d88-40ca-9765-48d48e7fe89f 34 fields · synced May 30, 2026