Ab Binder

FDA UDI

Class I (US FDA UDI)

by Pepper Medical, Inc.

Identity

Trade Name: Ab Binder FDA UDI
Generic Name: Abdominal binder, single-use FDA UDI
Device Name: Ab Binder, Large (3 Panel) FDA UDI
Model / Reference: AB360 FDA UDI
Description: Ab Binder, Large (3 Panel) FDA UDI

Identifiers

Catalog Number: AB360 FDA UDI
Primary DI / UDI-DI: 00850014574550 FDA UDI
FDA Product Code: FSD FDA UDI
GMDN Term: Abdominal binder, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.5160 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Safe FDA UDI

Category: Abdominal binder, single-use

Ab Binder by Pepper Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Abdominal binder, single-use.

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MATERNITY MATE LUMBOSACRAL 2XL — BIRD & CRONIN, LLC · Class I
12" ABDOMINAL BINDER UP TO 45" — BIRD & CRONIN, LLC · Class I
8" ABDOMINAL BINDER 42-48 IN. XL — BIRD & CRONIN, LLC · Class I
Novo Surgical Inc. — NOVO SURGICAL, INC. · Class I
Kendall — Cardinalhealth · Class I
PENDULOUS ABD LUMBO SUPPORT MD — BIRD & CRONIN, LLC · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Pepper Medical, Inc.

Sources (1)

FDA UDI fdc6c8fe-4a63-4fb0-8682-9a4333cbfd82 35 fields · synced Jun 8, 2026