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Tip Control

FDA UDI

Class I (US FDA UDI)

by Richard Wolf GmbH

Identity

Trade Name
TIP CONTROL FDA UDI
Generic Name
General-purpose surgical scissors, reusable FDA UDI
Device Name
SCISSORS Ø 5.2MM 482MM articulating, single opening, sheath straight, TL 644 mm, reusable FDA UDI
Model / Reference
823400003 FDA UDI
Description
SCISSORS Ø 5.2MM 482MM articulating, single opening, sheath straight, TL 644 mm, reusable FDA UDI

Identifiers

Catalog Number
823400003 FDA UDI
Primary DI / UDI-DI
04055207056431 FDA UDI
FDA Product Code
LRC FDA UDI
GMDN Term
General-purpose surgical scissors, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 5.2 Millimeter FDA UDI
Length — 482 Millimeter FDA UDI

Tip Control by Richard Wolf GmbH — 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

Manufacturer
Richard Wolf GmbH

Sources (1)

  • FDA UDI 92846822-5ea8-40f8-b4fa-6ae069cb6fec 38 fields · synced May 31, 2026