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Bowflex

FDA UDI

Class II (US FDA UDI)

by Taylor Precision Products, Inc.

Identity

Trade Name
Bowflex FDA UDI
Generic Name
Bioelectrical body composition analyser FDA UDI
Device Name
BODY COMPOSITION ANALYZERS FDA UDI
Model / Reference
0116 FDA UDI
Description
BODY COMPOSITION ANALYZERS FDA UDI

Identifiers

Catalog Number
57284072FBOW FDA UDI
Primary DI / UDI-DI
04897077350116 FDA UDI
FDA Product Code
MNW FDA UDI
GMDN Term
Bioelectrical body composition analyser FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2770 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

Category: Bioelectrical body composition analyser

Bowflex by Taylor Precision Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bioelectrical body composition analyser.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 856986ce-7168-4528-995f-047b9cf4560e 34 fields · synced Jun 8, 2026