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Gas Strut

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref MTRHGS01Model Thermoplastic Devices

by Medtec LLC

Identity

Trade Name
Gas Strut FDA UDI
Generic Name
Thermoplastic-moulding water bath FDA UDI
Device Name
Gas Strut FDA UDI
Model / Reference
MTRHGS01 EUDAMEDFDA UDI
Thermoplastic Devices EUDAMED
Description
Gas Strut FDA UDI

Identifiers

Catalog Number
MTRHGS01 FDA UDI
Primary DI / UDI-DI
00841439107195 EUDAMEDFDA UDI
Basic UDI-DI
8414391OC0003R01AA EUDAMED
510(k) Number
K933227 FDA UDI
FDA Product Code
IYE FDA UDI
EMDN Code
Y0699 EXTERNAL PROSTHESES AND ORTHOSES - OTHER EUDAMED
GMDN Term
Thermoplastic-moulding water bath FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
892.5050 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 16.9 Centimeter FDA UDI
Length — 46.8 Centimeter FDA UDI

Category: Thermoplastic-moulding water bath

Gas Strut by Medtec LLC — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Thermoplastic-moulding water bath.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medtec LLC

Sources (2)

  • FDA UDI 20ddacd8-4bf5-49e7-b2e3-31f7d240aafe 37 fields · synced Jun 19, 2026
  • EUDAMED d63dc8fb-dcc2-45a7-841f-8469cd98aad3 61 fields · synced Jun 19, 2026