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Xpect

FDA UDI

Class I (US FDA UDI)

by Cintas Corporation No. 2

Identity

Trade Name
Xpect FDA UDI
Generic Name
Surgical/examination garment kit FDA UDI
Device Name
Polymer Patient Exam Gloves Large FDA UDI
Model / Reference
182309 FDA UDI
Description
Polymer Patient Exam Gloves Large FDA UDI

Identifiers

Primary DI / UDI-DI
00850047958990 FDA UDI
FDA Product Code
LZA FDA UDI
GMDN Term
Surgical/examination garment kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6250 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical/examination garment kit

Xpect by Cintas Corporation No. 2 — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/examination garment kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5142eba7-fdf3-400e-ba35-137d1d0e385c 34 fields · synced May 30, 2026