Identity
- Trade Name
- SafeStraw™ 2 Pack FDA UDI
- Generic Name
- Assistive drinking straw FDA UDI
- Device Name
- SafeStraw™ 2 Pack FDA UDI
- Model / Reference
- 205 FDA UDI
- Description
- SafeStraw™ 2 Pack FDA UDI
Identifiers
- Catalog Number
- 205 FDA UDI
- Primary DI / UDI-DI
- 00714646000866 FDA UDI
- FDA Product Code
- ILC FDA UDI
- GMDN Term
- Assistive drinking straw FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5050 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
Yes
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Assistive drinking straw
SafeStraw™ 2 Pack by Bionix, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Assistive drinking straw.
- SafeStraw™ Variety Pack — Bionix, LLC · Class I
- SafeStraw — Bionix, LLC · Class I
- SafeStraw — Bionix, 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
- Bionix, LLC
Sources (1)
- FDA UDI 38eee2d7-8c73-4192-b4e7-00b0daa3b7d8 35 fields · synced May 30, 2026