Bam

FDA UDI

Class I (US FDA UDI)

by Ehob, Inc.

Identity

Trade Name: BAM FDA UDI
Generic Name: Patient transfer system, manual FDA UDI
Device Name: 25ft Inflation Hose Cover FDA UDI
Model / Reference: REV00 FDA UDI
Description: 25ft Inflation Hose Cover FDA UDI

Identifiers

Catalog Number: Z0156K1 FDA UDI
Primary DI / UDI-DI: 10603354130521 FDA UDI
FDA Product Code: FMR FDA UDI
GMDN Term: Patient transfer system, manual FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 880.6785 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

FDA UDI

MRI Safety

MR Safe FDA UDI

Category: Patient transfer system, manual

Bam by Ehob, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Ehob, Inc.

Sources (1)

FDA UDI 419c888b-f77a-46aa-82c5-2db68062100e 34 fields · synced May 31, 2026