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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
Dry-heat sterilizer FDA UDI
Device Name
Stainless Steel Sterilizer, Dry Heat FDA UDI
Model / Reference
8376 FDA UDI
Description
Stainless Steel Sterilizer, Dry Heat FDA UDI

Identifiers

Primary DI / UDI-DI
M36883761 FDA UDI
FDA Product Code
KMH FDA UDI
GMDN Term
Dry-heat sterilizer FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6870 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dry-heat sterilizer

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

Similar devices

Also classified as Dry-heat sterilizer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI edc56da7-0a8a-4ade-b0f9-86a1d5dc404e 34 fields · synced May 30, 2026