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Xpert

FDA UDI

Class I (US FDA UDI)

by Sempermed Usa, Inc.

Identity

Trade Name
Xpert FDA UDI
Generic Name
Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Device Name
Nitrile Exam Glove, PF size XXL FDA UDI
Model / Reference
SGXN 106 FDA UDI
Description
Nitrile Exam Glove, PF size XXL FDA UDI

Identifiers

Catalog Number
SGXN 106 FDA UDI
Primary DI / UDI-DI
00841277109054 FDA UDI
FDA Product Code
LZC FDA UDI
OPJ FDA UDI
QDO FDA UDI
LZA FDA UDI
GMDN Term
Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6250 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Xpert by Sempermed Usa, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sempermed Usa, Inc.

Sources (1)

  • FDA UDI b9639cc4-43d4-4553-9fd6-bb4c4fc32c9d 35 fields · synced May 31, 2026