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Grafco

FDA UDI

Class I (US FDA UDI)

by GF Health Products, Inc

Identity

Trade Name
Grafco FDA UDI
Generic Name
Bedpan FDA UDI
Device Name
FRACTURE BEDPAN G0LD- HANGING FDA UDI
Model / Reference
2302-B FDA UDI
Description
FRACTURE BEDPAN G0LD- HANGING FDA UDI

Identifiers

Catalog Number
2302-B FDA UDI
Primary DI / UDI-DI
M3682302B1 FDA UDI
FDA Product Code
FOB FDA UDI
GMDN Term
Bedpan FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6730 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bedpan

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

Similar devices

Also classified as Bedpan.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1e4ecefe-7762-4672-81e8-3404ec004b72 35 fields · synced May 31, 2026