← Back to catalogue

Vac-Lok™ Vacuum Compressor

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref MTVPEXCModel Vac-Lok Cushions

by Medtec LLC

Identity

Trade Name
Vac-Lok™ Vacuum Compressor FDA UDI
Generic Name
Vacuum-mould patient positioning system FDA UDI
Device Name
Dual function 230V compressor with hand control FDA UDI
Model / Reference
MTVPEXC EUDAMEDFDA UDI
Vac-Lok Cushions EUDAMED
Description
Dual function 230V compressor with hand control FDA UDI

Identifiers

Catalog Number
MTVPEXC FDA UDI
Primary DI / UDI-DI
00841439108734 EUDAMEDFDA UDI
Basic UDI-DI
8414391OC0018R13BX EUDAMED
510(k) Number
K935300 FDA UDI
FDA Product Code
IYE FDA UDI
EMDN Code
Z12011299 PATIENT POSITIONING INSTRUMENTS – OTHER EUDAMED
GMDN Term
Vacuum-mould patient positioning system 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Vacuum-mould patient positioning system

Vac-Lok™ Vacuum Compressor by Medtec LLC — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Vacuum-mould patient positioning system.

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 93ab9912-abb8-4c47-a7e9-51a25be4cba0 36 fields · synced Jul 23, 2026
  • EUDAMED d95a6a46-1ef8-4aca-a99e-67e3315f9685 61 fields · synced Jul 23, 2026