Identity
- Trade Name
- Acanthus FDA UDI
- Generic Name
- Personal device holder, single-use FDA UDI
- Device Name
- Acanthus Nasal Cannula Holder Case of 10 FDA UDI
- Model / Reference
- ANCH01980010 FDA UDI
- Description
- Acanthus Nasal Cannula Holder Case of 10 FDA UDI
Identifiers
- Catalog Number
- ANCH01980010 FDA UDI
- Primary DI / UDI-DI
- 00860010190845 FDA UDI
- FDA Product Code
- JAY FDA UDI
- GMDN Term
- Personal device holder, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5280 FDA UDI
- Commercial Distribution
- Not 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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Acanthus by Acanthus Medical Creations, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Acanthus Medical Creations, Llc
Sources (1)
- FDA UDI 963e99d9-4d81-426e-a2b1-e5616cea9cda 35 fields · synced May 30, 2026