Identity
- Trade Name
- CARDINAL HEALTH FDA UDI
- Generic Name
- Amniocentesis kit, medicated, single-use FDA UDI
- Device Name
- AMNIOCENTESIS 20GX3,5 DF FDA UDI
- Model / Reference
- 29-AM1CODF FDA UDI
- Description
- AMNIOCENTESIS 20GX3,5 DF FDA UDI
Identifiers
- Catalog Number
- 29-AM1CODF FDA UDI
- Primary DI / UDI-DI
- 10887488293608 FDA UDI
- FDA Product Code
- HIO FDA UDI
- GMDN Term
- Amniocentesis kit, medicated, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 884.1550 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Category: Amniocentesis kit, medicated, single-use
Cardinal Health by Cardinal Health 200, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Amniocentesis kit, medicated, single-use.
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- CARDINAL HEALTH — Cardinal Health 200, LLC · Class II
- CARDINAL HEALTH — Cardinal Health 200, 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 |
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Manufacturer
- Manufacturer
- Cardinal Health 200, LLC
Sources (1)
- FDA UDI 0d1eaef9-56a0-4c42-a833-41ea47e11aec 35 fields · synced Jun 8, 2026