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H-E-B

FDA UDI

Class I (US FDA UDI)

by H. E. Butt Grocery Company

Identity

Trade Name
H-E-B FDA UDI
Generic Name
Non-woven gauze pad FDA UDI
Device Name
Large Gauze Pads, 4 IN x 4 IN (101 mm x 101 mm) FDA UDI
Model / Reference
041220290086 FDA UDI
Description
Large Gauze Pads, 4 IN x 4 IN (101 mm x 101 mm) FDA UDI

Identifiers

Primary DI / UDI-DI
00041220290086 FDA UDI
FDA Product Code
NAB FDA UDI
GMDN Term
Non-woven gauze pad 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

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Non-woven gauze pad

H-E-B by H. E. Butt Grocery Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-woven gauze pad.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2b841d9d-35d1-4376-a0f3-c27e817687a0 33 fields · synced May 31, 2026