← Back to catalogue

Globe

FDA UDI

Class I (US FDA UDI)

by Trifecta Pharmaceuticals USA LLC

Identity

Trade Name
Globe FDA UDI
Generic Name
Woven gauze pad, non-antimicrobial FDA UDI
Device Name
Globe Sterile Gauze Pads 3 x 3 Box of 100 FDA UDI
Model / Reference
20202 FDA UDI
Description
Globe Sterile Gauze Pads 3 x 3 Box of 100 FDA UDI

Identifiers

Primary DI / UDI-DI
00850026393064 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

No

FDA UDI

Category: Woven gauze pad, non-antimicrobial

Globe by Trifecta Pharmaceuticals USA 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Trifecta Pharmaceuticals USA LLC

Sources (1)

  • FDA UDI 58c6e431-74c8-4e14-b1bf-185c55a1931c 34 fields · synced May 30, 2026