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PEIPU Patient Nitrile Examination Gloves blue1

FDA UDI

Class I (US FDA UDI)

by shenzhenshishentongdianziyouxiangongsi

Identity

Trade Name
PEIPU Patient Nitrile Examination Gloves blue1 FDA UDI
Generic Name
Nitrile examination/treatment glove, non-powdered, non-antimicrobial FDA UDI
Device Name
Disposable nitrile gloves are made from butadiene rubber latex by vulcanizing, dipping and drying.It is applicable to the general medical examination of the hospital. FDA UDI
Model / Reference
Standard40 FDA UDI
Description
Disposable nitrile gloves are made from butadiene rubber latex by vulcanizing, dipping and drying.It is applicable to the general medical examination of the hospital. FDA UDI

Identifiers

Primary DI / UDI-DI
16975878910403 FDA UDI
510(k) Number
K121526 FDA UDI
FDA Product Code
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
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

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: Nitrile examination/treatment glove, non-powdered, non-antimicrobial

PEIPU Patient Nitrile Examination Gloves blue1 by shenzhenshishentongdianziyouxiangongsi — Class I — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Nitrile examination/treatment glove, non-powdered, non-antimicrobial.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 018950ad-f7fd-4f39-9c34-ea36bf79c341 34 fields · synced Jun 8, 2026