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Mh

FDA UDI

Class I (US FDA UDI)

by Mazza Healthcare LLC

Identity

Trade Name
MH FDA UDI
Generic Name
Surgical instrument guard, single-use FDA UDI
Device Name
CSR Wrap Closure Tape, 2.5cm x 50m, non-sterile FDA UDI
Model / Reference
97-0250-AT FDA UDI
Description
CSR Wrap Closure Tape, 2.5cm x 50m, non-sterile FDA UDI

Identifiers

Primary DI / UDI-DI
10850018327975 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Surgical instrument guard, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical instrument guard, single-use

Mh by Mazza Healthcare LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical instrument guard, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 75d082b6-6afa-4b0d-87c9-8e9e093adf7b 33 fields · synced May 31, 2026