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Grafco

FDA UDI

Class II (US FDA UDI)

by GF Health Products, Inc

Identity

Trade Name
Grafco FDA UDI
Generic Name
Cytology scraper, single-use FDA UDI
Device Name
Cervical Scrapers FDA UDI
Model / Reference
1601 FDA UDI
Description
Cervical Scrapers FDA UDI

Identifiers

Primary DI / UDI-DI
M36816011 FDA UDI
FDA Product Code
HHT FDA UDI
GMDN Term
Cytology scraper, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4530 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cytology scraper, single-use

Grafco by GF Health Products, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cytology scraper, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f6b311ad-d18a-4235-8c1f-cfe1528abfb0 34 fields · synced May 30, 2026