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EUDAMED last updated this device on Mar 17, 2026
0759265DEXIIXATeeter is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by STL International, Inc.; DBA-Teeter. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
00759265000019Dex II(01)00759265000019
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z12130201TRACTION BEDS1 warning recorded — scroll inside the panel to see all entries.
Consult healthcare professional before Use-Inversion therapy should not be used without a physician approval, as it is contraindicated for any medical or health condition that could be aggravated by increased blood pressure, intracranial pressure, or mechanical stress from inversion, or that could impair the user's ability to operate the equipment safely. This includes, but is not limited to, any neurological or other condition causing unexplained tingling, weakness, neuropathy, seizure, sleep disorder, lightheadedness, dizziness, disorientation, fatigue, or impairments to strength, mobility, alertness, or cognitive function; any brain condition such as trauma, history of intracranial bleeding, transient ischemic attack (TIA) or stroke, or severe headaches; any heart or circulatory disorder such as high blood pressure, hypertension, increased stroke risk, or use of anticoagulants (including high-dose aspirin); any bone, skeletal, or spinal cord condition or injury such as significant spinal curvature, acutely swollen joints, osteoporosis, fractures, dislocations, medullary pins, or surgically implanted orthopedic supports; any eye, ear, nasal, or balance condition such as trauma, history of retinal detachment, glaucoma, optic hypertension, chronic sinusitis, middle or inner ear disease, motion sickness, or vertigo; any digestive or internal disorder such as severe acid reflux, hiatal or other hernia, or gallbladder or kidney disease; and any condition for which exercise is specifically restricted or prohibited by a physician, such as pregnancy, obesity, or recent surgeries
Primary placement in Germany; available across 1 country total.
Placed on the market in Germany; per-country availability dates not published.
US-MF-000024237The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.No certificate specifically references this device's Basic UDI-DI.