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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
Wound-nonadherent dressing, absorbent, non-antimicrobial FDA UDI
Device Name
Non-Stick Pads, 3 IN x 4 IN (76 mm x 101 mm) FDA UDI
Model / Reference
041220032259 FDA UDI
Description
Non-Stick Pads, 3 IN x 4 IN (76 mm x 101 mm) FDA UDI

Identifiers

Primary DI / UDI-DI
00041220032259 FDA UDI
FDA Product Code
NAC FDA UDI
GMDN Term
Wound-nonadherent dressing, absorbent, non-antimicrobial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4018 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: Wound-nonadherent dressing, absorbent, non-antimicrobial

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 Wound-nonadherent dressing, absorbent, non-antimicrobial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0805f2f3-d3ab-4e99-8f5e-c53a9c4fdb10 33 fields · synced Jun 1, 2026