← Back to catalogue
Replacement String Pull Cord 12/Pack For Iq Magnetic
FDA UDIClass I (US FDA UDI)
by AliMed, LLC
Identity
- Trade Name
- REPLACEMENT STRING PULL CORD 12/PACK FOR IQ MAGNETIC FDA UDI
- Generic Name
- Vulnerable patient home alert system FDA UDI
- Model / Reference
- 72226 FDA UDI
Identifiers
- Catalog Number
- 2970009627 FDA UDI
- Primary DI / UDI-DI
- 00733657228090 FDA UDI
- FDA Product Code
- KMI FDA UDI
- GMDN Term
- Vulnerable patient home alert system FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.2400 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
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
Yes
FDA UDI
Category: Vulnerable patient home alert system
Replacement String Pull Cord 12/Pack For Iq Magnetic by AliMed, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Vulnerable patient home alert system.
- HomeSafe Standard Personal Help Pendant — Lifeline Systems, Inc. · Class II
- Senior Living Alert Device AutoAlert with Indicator — Lifeline Systems, Inc. · Class II
- Philips BlueBand — Lifeline Systems, Inc. · Class II
- MEDLINE — MEDLINE INDUSTRIES, INC. · Class I
- Fall monitor — Securitas Healthcare LLC · Class I
- Senior Living Alert DevicePersonal Help Pendant — Lifeline Systems, Inc. · Class II
- HomeSafe AutoAlert Pendant — Lifeline Systems, Inc. · Class II
- HomeSafe Standard Home Communicator — Lifeline Systems, Inc. · Class II
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- AliMed, LLC
Sources (1)
- FDA UDI 0ce3d701-72f8-49de-bf63-8c92415d85cd 34 fields · synced Jun 9, 2026