Reli-Cut®

FDA UDI

Class I (US FDA UDI)

by Myco Medical Supplies Inc.

Identity

Trade Name: RELI-CUT® FDA UDI
Generic Name: Scalpel, single-use FDA UDI
Device Name: RELI-CUT® #20 Retractable Blade Safety Scalpel, Bulk, Non-Sterile, 1000/CS FDA UDI
Model / Reference: 6000CSTR-20 FDA UDI
Description: RELI-CUT® #20 Retractable Blade Safety Scalpel, Bulk, Non-Sterile, 1000/CS FDA UDI

Identifiers

Catalog Number: 6000CSTR-20 FDA UDI
Primary DI / UDI-DI: 10386120011056 FDA UDI
FDA Product Code: GES FDA UDI
GMDN Term: Scalpel, 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Ethylene Oxide FDA UDI

Category: Scalpel, single-use

Reli-Cut® by Myco Medical Supplies Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Scalpel, single-use.

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comknife® — Beijing Bohai Kangyuan Medical Devices Co., Ltd. · Class I
Bard-Parker ® Disposable Scalpels — Aspen Surgical Products, Inc. · Class I
Sharpoint — Surgical Specialties México, S. de R.L. de C.V. · Class I
comknife® — Beijing Bohai Kangyuan Medical Devices Co., Ltd. · Class I
Stylus — Surgical Specialties México, S. de R.L. de C.V. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Myco Medical Supplies Inc.

Sources (1)

FDA UDI 2b4562ef-6803-425c-b0d5-647c6470364f 34 fields · synced May 30, 2026