Identity
- Trade Name
- CareFusion 2200 FDA UDI
- Generic Name
- Suturing unit, reprocessed FDA UDI
- Model / Reference
- RH1145-004 FDA UDI
Identifiers
- Primary DI / UDI-DI
- B504GSRH11450040 FDA UDI
- FDA Product Code
- KDC FDA UDI
- GMDN Term
- Suturing unit, reprocessed FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 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
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
Yes
FDA UDI
Category: Suturing unit, reprocessed
CareFusion 2200 by Provision — 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
- Provision
Sources (1)
- FDA UDI 3be9103e-0c1f-4c79-ac82-d6bc69799afc 33 fields · synced May 30, 2026