Identity
- Trade Name
- Safe-T-Centesis FDA UDI
- Generic Name
- Aspiration tray, single-use FDA UDI
- Device Name
- Safe-T-Centesis PLUS 8 Fr Catheter Drainage Tray FDA UDI
- Model / Reference
- PIG1280TSP FDA UDI
- Description
- Safe-T-Centesis PLUS 8 Fr Catheter Drainage Tray FDA UDI
Identifiers
- Catalog Number
- PIG1280TSP FDA UDI
- Primary DI / UDI-DI
- 10885403108426 FDA UDI
- FDA Product Code
- PXI FDA UDI
- GMDN Term
- Aspiration tray, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5570 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
Yes
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: Aspiration tray, single-use
Safe-T-Centesis by Carefusion 2200, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Aspiration tray, single-use.
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- Turkel — Cardinalhealth · Class II
- Safe-T-Centesis — CAREFUSION 2200, INC. · Class II
- PercuSet Basic Biopsy Tray — Bracco Diagnostics Inc. · 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 II | Pending data |
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Manufacturer
- Manufacturer
- Carefusion 2200, Inc
Sources (1)
- FDA UDI dfcc7443-051b-41ec-87d5-9d0651759595 36 fields · synced Jun 8, 2026