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SafeClean ® Hand/Nail Brushes

FDA UDI

Class I (US FDA UDI)

by Aspen Surgical Products, Inc.

Identity

Trade Name
SafeClean ® Hand/Nail Brushes FDA UDI
Generic Name
Surgical scrub brush, single-use FDA UDI
Device Name
Intended to remove surgical residue from surgical instruments and endoscopic devices after surgical procedures FDA UDI
Model / Reference
244001BBG FDA UDI
Description
Intended to remove surgical residue from surgical instruments and endoscopic devices after surgical procedures FDA UDI

Identifiers

Primary DI / UDI-DI
00840113209811 FDA UDI
FDA Product Code
MNL FDA UDI
GMDN Term
Surgical scrub brush, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.1500 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

Yes

FDA UDI

Category: Surgical scrub brush, single-use

SafeClean ® Hand/Nail Brushes by Aspen Surgical Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical scrub brush, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Aspen Surgical Products, Inc.

Sources (1)

  • FDA UDI 5b3d94e7-b771-47c2-b5c5-a89534dd79d0 34 fields · synced Jun 9, 2026