Identity
- Trade Name
- Acu-Life (HE) FDA UDI
- Generic Name
- Pill crusher/splitter FDA UDI
- Device Name
- PILL SPLITTER/CRUSHER 6/72 FDA UDI
- Model / Reference
- 400087 FDA UDI
- Description
- PILL SPLITTER/CRUSHER 6/72 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00079573100912 FDA UDI
- FDA Product Code
- OHY FDA UDI
- GMDN Term
- Pill crusher/splitter FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.6430 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Pill crusher/splitter
Acu-Life (HE) by Apothecary Products, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Apothecary Products, Inc.
Sources (1)
- FDA UDI 9d072002-b268-47eb-a5e7-b233609ff84b 34 fields · synced Jun 1, 2026