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Sklar®

FDA UDI

Class I (US FDA UDI)

by Sklar Corporation

Identity

Trade Name
Sklar® FDA UDI
Generic Name
Vascular scissors FDA UDI
Device Name
TOLEDO VASC MICRO SCISS 7MM25° FDA UDI
Model / Reference
98-9415 FDA UDI
Description
TOLEDO VASC MICRO SCISS 7MM25° FDA UDI

Identifiers

Primary DI / UDI-DI
10649111345838 FDA UDI
FDA Product Code
LRW FDA UDI
GMDN Term
Vascular scissors 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Vascular scissors

Sklar Sklar® is a high-quality, reusable hand-held surgical instrument designed for cutting blood vessels during open vascular surgery. This versatile device features two small pivoted blades that cut with a shearing action, allowing for precise and controlled vessel penetration. With its metallic construction and adjustable blade angle, the Vascular Scissors are ideal for use in various medical procedures.

Similar devices

Also classified as Vascular scissors.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sklar Corporation

Sources (1)

  • FDA UDI 99313d74-4ff8-4564-b5c3-9e0cd787224c 33 fields · synced Jun 25, 2026