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Mastel Surgical

FDA UDI

Class I (US FDA UDI)

by International Surgical Products Inc

Identity

Trade Name
Mastel Surgical FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
INSTRUMENT TRAY ASSEMBLY 10 X 6 X .75 FDA UDI
Model / Reference
CP1038S-SB FDA UDI
Description
INSTRUMENT TRAY ASSEMBLY 10 X 6 X .75 FDA UDI

Identifiers

Catalog Number
AT0190 FDA UDI
Primary DI / UDI-DI
00810147255801 FDA UDI
FDA Product Code
LRP FDA UDI
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Instrument tray, reusable

Mastel Surgical by International Surgical Products Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Instrument tray, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bf7de68e-3f4e-434e-bd47-e503a0bc8df7 34 fields · synced Jun 8, 2026