Identity
- Trade Name
- WALGREENS FDA UDI
- Generic Name
- Axillary crutch FDA UDI
- Device Name
- Crutches (1 Pair) FDA UDI
- Model / Reference
- 586529 FDA UDI
- Description
- Crutches (1 Pair) FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00311917212722 FDA UDI
- FDA Product Code
- IPR FDA UDI
- GMDN Term
- Axillary crutch FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.3150 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Axillary crutch
Walgreens by Walgreen Co. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Axillary crutch.
- Probasics — COMPASS HEALTH BRANDS CORP. · Class I
- Wenzellite — Drive Devilbiss Healthcare · Class I
- PremierPro — SVS LLC · Class I
- Henry Schein — HENRY SCHEIN, INC. · Class I
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class I
- Probasics — COMPASS HEALTH BRANDS CORP. · Class I
- CARDINAL HEALTH — Cardinal Health 200, LLC · Class I
- PremierPro — SVS LLC · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Walgreen Co.
Sources (1)
- FDA UDI 53e90dd6-e3d0-4afd-af2a-13bd504d4e17 33 fields · synced Jun 1, 2026