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Critter Stabilization Device
EUDAMEDFDA UDIClass I (EU MDR)
Ref EKM-CSD10573
by Ekcomed Inc.
Identity
- Trade Name
- Critter Stabilization Device EUDAMEDEKCOMED FDA UDI
- Generic Name
- Limb/torso/head restraint, single-use FDA UDI
- Device Name
- Positioning Products EUDAMEDCritter Stabilization Device FDA UDI
- Model / Reference
- EKM-CSD10573 EUDAMEDFDA UDI
- Description
- Critter Stabilization Device FDA UDI
Identifiers
- Catalog Number
- EKM-CSD10573 FDA UDI
- Primary DI / UDI-DI
- 00850000965034 EUDAMEDFDA UDI
- Basic UDI-DI
- 0850000965positionYS EUDAMED
- Direct Marketing DI
- 00850000965034 EUDAMED
- FDA Product Code
- CCX FDA UDI
- EMDN Code
- Z12130285 ORTHOPAEDIC TRACTION INSTRUMENTS - CONSUMABLES EUDAMED
- GMDN Term
- Limb/torso/head restraint, single-use FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 868.6820 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Ethylene Oxide FDA UDI
Critter Stabilization Device by Ekcomed Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 0850000965positionYS | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Ekcomed Inc.
- EUDAMED SRN
- US-MF-000048880
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (2)
- EUDAMED 2759845c-9037-4b53-993e-530c2b45c20b 61 fields · synced Jul 9, 2026
- FDA UDI 5baf22e4-4b7e-4994-9656-c7894c71f6d8 35 fields · synced May 29, 2026