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FusionMax

FDA UDI

Class I (US FDA UDI)

by Surgix Medical Llc

Identity

Trade Name
FusionMax FDA UDI
Generic Name
Medical equipment/instrument drape, single-use FDA UDI
Device Name
Flex Frame Disposables Covers Kit - 2 fabric pad covers & 2 foam bar covers. Case of 20 FDA UDI
Model / Reference
FF-30017 FDA UDI
Description
Flex Frame Disposables Covers Kit - 2 fabric pad covers & 2 foam bar covers. Case of 20 FDA UDI

Identifiers

Catalog Number
FF-33017 FDA UDI
Primary DI / UDI-DI
00840343725327 FDA UDI
FDA Product Code
KME FDA UDI
GMDN Term
Medical equipment/instrument drape, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6060 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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: Medical equipment/instrument drape, single-use

FusionMax by Surgix Medical Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical equipment/instrument drape, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Surgix Medical Llc

Sources (1)

  • FDA UDI b5b36259-5f0b-4116-a5a3-29b1c7a0eda5 35 fields · synced Jun 1, 2026