Identity
- Trade Name
- Reticcount FDA UDI
- Generic Name
- Reticulocyte count IVD, control FDA UDI
- Device Name
- BD Retic-Count™ Control FDA UDI
- Model / Reference
- 340999 FDA UDI
- Description
- BD Retic-Count™ Control FDA UDI
Identifiers
- Catalog Number
- 340999 FDA UDI
- Primary DI / UDI-DI
- 00382903409990 FDA UDI
- FDA Product Code
- JPK FDA UDI
- GMDN Term
- Reticulocyte count IVD, control FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 864.8625 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
No
FDA UDI
Convenience Kit
Yes
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
Category: Reticulocyte count IVD, control
Reticcount by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Liquichek — Bio-Rad Laboratories · Class II
- Liquichek — Bio-Rad Laboratories · Class II
- Liquichek — Bio-Rad Laboratories · Class II
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 II | Pending data |
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Manufacturer
- Manufacturer
- Becton Dickinson And Company
Sources (1)
- FDA UDI 0f63d0ec-29bf-4b67-83e8-15e6ab6cfcfc 36 fields · synced May 30, 2026