Orthomed

FDA UDI

Class I (US FDA UDI)

by Ortho-Med, Inc.

Identity

Trade Name: ORTHOMED FDA UDI
Generic Name: General-purpose surgical scissors, reusable FDA UDI
Device Name: TC MAYO SCISSORS 9" CVD FDA UDI
Model / Reference: OM 35-0630 FDA UDI
Description: TC MAYO SCISSORS 9" CVD FDA UDI

Identifiers

Primary DI / UDI-DI: B8033506300 FDA UDI
FDA Product Code: HRR FDA UDI
GMDN Term: General-purpose surgical scissors, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4540 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

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

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: General-purpose surgical scissors, reusable

Orthomed by Ortho-Med, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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MILLENNIUM — AVALIGN TECHNOLOGIES, Inc. · Class I
Tecomet — Tecomet,Inc · Class I

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 I	Pending data

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Manufacturer

Manufacturer: Ortho-Med, Inc.

Sources (1)

FDA UDI 1654c19e-896b-4e3c-b7fc-b607b007de25 33 fields · synced Jun 8, 2026