Identity
- Trade Name
- Protective Mitt FDA UDI
- Generic Name
- Limb/torso/head restraint, single-use FDA UDI
- Device Name
- The Mitt is intended to be used to limit the movement of the patient's hands and fingers. FDA UDI
- Model / Reference
- Patient Protective Mitt Child w/o Stays FDA UDI
- Description
- The Mitt is intended to be used to limit the movement of the patient's hands and fingers. FDA UDI
Identifiers
- Catalog Number
- 50-1010 FDA UDI
- Primary DI / UDI-DI
- M1435010101 FDA UDI
- FDA Product Code
- FMQ FDA UDI
- GMDN Term
- Limb/torso/head restraint, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6760 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Limb/torso/head restraint, single-use
Protective Mitt by Kenad Sg Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Kenad Sg Medical, Inc.
Sources (1)
- FDA UDI aca8b5a7-2e0a-4cc3-b242-273ed6032c2f 35 fields · synced May 30, 2026