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Medi-Cut Blades #22

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Medi-Cut Blades #22 FDA UDI
Generic Name
Manual scalpel blade, single-use FDA UDI
Model / Reference
4142 FDA UDI

Identifiers

Primary DI / UDI-DI
00616784414225 FDA UDI
FDA Product Code
GES FDA UDI
GMDN Term
Manual scalpel blade, single-use 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

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Manual scalpel blade, single-use

Medi-Cut Blades #22 is a high-quality, single-use manual scalpel blade designed for general surgical applications. The device features a durable stainless steel alloy construction, a retractable protective guard, and a precise cutting edge that effectively dissects tissues. With its implantable safety mechanisms and update history, this device is suitable for medical professionals in need of a reliable, sterile tool.

Similar devices

Also classified as Manual scalpel blade, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI 04733501-d95f-4181-b818-0c9f889c3753 32 fields · synced Jul 26, 2026