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Tenotomy Scissors, Straight Jaw, Ring Handle, Thin Blades, 11cm

FDA UDI

Class I (US FDA UDI)

by Mizuho America, Inc.

Identity

Trade Name
Tenotomy Scissors, Straight Jaw, Ring Handle, Thin Blades, 11cm FDA UDI
Generic Name
General-purpose surgical scissors, reusable FDA UDI
Device Name
Actuated Cutting FDA UDI
Model / Reference
99-600-33 FDA UDI
Description
Actuated Cutting FDA UDI

Identifiers

Primary DI / UDI-DI
00810009465492 FDA UDI
FDA Product Code
LRW FDA UDI
GMDN Term
General-purpose surgical scissors, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
Not 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

No

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

Tenotomy Scissors, Straight Jaw, Ring Handle, Thin Blades, 11cm by Mizuho America, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 01f6b711-d885-4268-9e4f-318f354d3ebf 34 fields · synced Jun 1, 2026