← Back to catalogue

LW Scientific, Inc.

FDA UDI

Class I (US FDA UDI)

by Lw Scientific, Inc.

Identity

Trade Name
LW Scientific, Inc. FDA UDI
Generic Name
Paraffin wax bath FDA UDI
Device Name
Ready Warm tissue floatation bath FDA UDI
Model / Reference
FWL-TISS-BTH3 FDA UDI
Description
Ready Warm tissue floatation bath FDA UDI

Identifiers

Catalog Number
FWL-TISS-BTH3 FDA UDI
Primary DI / UDI-DI
00664816005842 FDA UDI
FDA Product Code
IDY FDA UDI
GMDN Term
Paraffin wax bath FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3010 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Paraffin wax bath

LW Scientific, Inc. by Lw Scientific, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Paraffin wax bath.

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
Lw Scientific, Inc.

Sources (1)

  • FDA UDI c2792b12-653e-4111-94e9-723ee4046b32 34 fields · synced May 30, 2026