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Pocket Nurse

FDA UDI

Class I (US FDA UDI)

by Pocket Nurse Enterprises, Inc.

Identity

Trade Name
Pocket Nurse FDA UDI
Generic Name
Vinyl examination/treatment glove, non-powdered FDA UDI
Device Name
Pocket Nurse Glove Exam Synthetic Vinyl Non-Sterile - Medium FDA UDI
Model / Reference
03-47-1600-MED FDA UDI
Description
Pocket Nurse Glove Exam Synthetic Vinyl Non-Sterile - Medium FDA UDI

Identifiers

Primary DI / UDI-DI
10197644487216 FDA UDI
FDA Product Code
KGO FDA UDI
GMDN Term
Vinyl examination/treatment glove, non-powdered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4460 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Vinyl examination/treatment glove, non-powdered

Pocket Nurse by Pocket Nurse Enterprises, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pocket Nurse Enterprises, Inc.

Sources (1)

  • FDA UDI cc67a3f8-116a-4fd6-9c53-0b03c50af464 33 fields · synced May 31, 2026