Robbins Disposable Dermal Curettes

FDA UDI

Class I (US FDA UDI)

by Robbins Instruments

Identity

Trade Name: Robbins Disposable Dermal Curettes FDA UDI
Generic Name: Dermal curette, single-use FDA UDI
Device Name: Robbins Disposable Dermal Curettes 2,3,4,5,7mm FDA UDI
Model / Reference: RDC-A FDA UDI
Description: Robbins Disposable Dermal Curettes 2,3,4,5,7mm FDA UDI

Identifiers

Catalog Number: RDC-A FDA UDI
Primary DI / UDI-DI: 90850010779273 FDA UDI
FDA Product Code: FZS FDA UDI
GMDN Term: Dermal curette, 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Radiation Sterilization FDA UDI

Category: Dermal curette, single-use

Robbins Disposable Dermal Curettes by Robbins Instruments — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Robbins Instruments

Sources (1)

FDA UDI cb413b25-0e2f-4e24-929d-8116afe8a031 35 fields · synced Jun 8, 2026