← Back to catalogue

Waterbath

FDA UDI

Class I (US FDA UDI)

by Medtec LLC

Identity

Trade Name
Waterbath FDA UDI
Generic Name
Thermoplastic-moulding water bath FDA UDI
Device Name
120V FDA UDI
Model / Reference
MTRH1500 FDA UDI
Description
120V FDA UDI

Identifiers

Catalog Number
MTRH1500 FDA UDI
Primary DI / UDI-DI
00841439111338 FDA UDI
FDA Product Code
KPY FDA UDI
GMDN Term
Thermoplastic-moulding water bath FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.6500 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

Yes

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

Yes

FDA UDI

Category: Thermoplastic-moulding water bath

Waterbath by Medtec LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Thermoplastic-moulding water 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
Medtec LLC

Sources (1)

  • FDA UDI 7175bce2-a0f7-42c0-810e-cd9cb1110dae 35 fields · synced May 30, 2026