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Scalpel Handle

FDA UDI

Class I (US FDA UDI)

by Ovation International

Identity

Trade Name
Scalpel Handle FDA UDI
Generic Name
Scalpel handle, reusable FDA UDI
Device Name
TROUTMAN RAZOR BLADE HOLDER 5.5 MM HANDLE, STRAIGHT FDA UDI
Model / Reference
OI-2306T FDA UDI
Description
TROUTMAN RAZOR BLADE HOLDER 5.5 MM HANDLE, STRAIGHT FDA UDI

Identifiers

Primary DI / UDI-DI
08903317030864 FDA UDI
FDA Product Code
GDZ FDA UDI
GMDN Term
Scalpel handle, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Scalpel handle, reusable

Scalpel Handle by Ovation International — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Scalpel handle, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7d785682-2ef4-48b5-8a75-066f648a6877 33 fields · synced Jun 1, 2026