Identity
- Trade Name
- Large Left Arm Anchor FDA UDI
- Generic Name
- Assistive suction cup stabilizer/hand-hold FDA UDI
- Device Name
- Arm Anchor FDA UDI
- Model / Reference
- K814 FDA UDI
- Description
- Arm Anchor FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00858101008360 FDA UDI
- FDA Product Code
- KID FDA UDI
- GMDN Term
- Assistive suction cup stabilizer/hand-hold FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3910 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
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
Category: Assistive suction cup stabilizer/hand-hold
Large Left Arm Anchor by Rifton Equipment — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Assistive suction cup stabilizer/hand-hold.
- Large Right Arm Anchor — RIFTON EQUIPMENT · Class I
- Hand Anchor — RIFTON EQUIPMENT · Class I
- Wrist Anchor — RIFTON EQUIPMENT · Class I
- Grab Bar — RIFTON EQUIPMENT · Class I
- Right Elbow Anchor — RIFTON EQUIPMENT · Class I
- Left Elbow Anchor — RIFTON EQUIPMENT · Class I
- Small Left Arm Anchor — RIFTON EQUIPMENT · Class I
- Horizontal Anchor — RIFTON EQUIPMENT · Class I
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
- Rifton Equipment
Sources (1)
- FDA UDI 8aee3795-8ac3-4042-ac14-af22b1c28fa4 33 fields · synced Jun 8, 2026