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Exact Medical Manufacturing, Inc.

FDA UDI

Class I (US FDA UDI)

by Exact Medical Manufacturing

Identity

Trade Name
Exact Medical Manufacturing, Inc. FDA UDI
Generic Name
Patient surgical drape, single-use FDA UDI
Device Name
ScatterPro FDA UDI
Model / Reference
EN-RF-001 FDA UDI
Description
ScatterPro FDA UDI

Identifiers

Catalog Number
EN-RF-001 FDA UDI
Primary DI / UDI-DI
06975424195073 FDA UDI
FDA Product Code
KPY FDA UDI
GMDN Term
Patient surgical drape, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.6500 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

No

FDA UDI

Over-the-Counter

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Patient surgical drape, single-use

Exact Medical Manufacturing, Inc. by Exact Medical Manufacturing — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Patient surgical drape, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI db740c15-1690-4a55-bd9d-e7e677dd31f0 34 fields · synced Jun 1, 2026