← Back to catalogue

Bam

FDA UDI

Class I (US FDA UDI)

by Ehob, Inc.

Identity

Trade Name
BAM FDA UDI
Generic Name
General-purpose patient lifting system sling/harness FDA UDI
Device Name
BAM Air LC (RS/CTES) 1 Qty - Single Packed FDA UDI
Model / Reference
REV00 FDA UDI
Description
BAM Air LC (RS/CTES) 1 Qty - Single Packed FDA UDI

Identifiers

Catalog Number
B0166B1 FDA UDI
Primary DI / UDI-DI
10603354130347 FDA UDI
FDA Product Code
FMR FDA UDI
FSA FDA UDI
GMDN Term
General-purpose patient lifting system sling/harness FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6785 FDA UDI
880.5510 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: General-purpose patient lifting system sling/harness

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

Similar devices

Also classified as General-purpose patient lifting system sling/harness.

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
Ehob, Inc.

Sources (1)

  • FDA UDI 15d6974d-e03c-464d-8920-d8fb06b146bb 34 fields · synced May 30, 2026