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P&P Medical Surgical LLC

FDA UDI

Class I (US FDA UDI)

by P&P Medical Surgical LLC

Identity

Trade Name
P&P Medical Surgical LLC FDA UDI
Generic Name
Woven gauze pad, non-antimicrobial FDA UDI
Device Name
Gauze Surgical Sponges Cotton NON STERILE Woven 8-ply High Grade Quality 4"x4" Class I(a) All Purpose Pads Pack of 100 FDA UDI
Model / Reference
07150 FDA UDI
Description
Gauze Surgical Sponges Cotton NON STERILE Woven 8-ply High Grade Quality 4"x4" Class I(a) All Purpose Pads Pack of 100 FDA UDI

Identifiers

Primary DI / UDI-DI
G026071501 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Woven gauze pad, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4014 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Woven gauze pad, non-antimicrobial

P&P Medical Surgical LLC by P&P Medical Surgical LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Woven gauze pad, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 160dde45-b574-468a-a781-c16f4461fad9 33 fields · synced May 31, 2026