Identity
- Trade Name
- Snowden-Pencer FDA UDI
- Generic Name
- Suturing needle holder, reusable FDA UDI
- Device Name
- Snowden-Pencer Cardiovascular DIAMOND-JAW NEEDLE HOLDERS HEANEY 20.5CM (8"), 2500 JAW FDA UDI
- Model / Reference
- 32-0230 FDA UDI
- Description
- Snowden-Pencer Cardiovascular DIAMOND-JAW NEEDLE HOLDERS HEANEY 20.5CM (8"), 2500 JAW FDA UDI
Identifiers
- Catalog Number
- 32-0230 FDA UDI
- Primary DI / UDI-DI
- 10885403143939 FDA UDI
- FDA Product Code
- DWS FDA UDI
- GMDN Term
- Suturing needle holder, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 870.4500 FDA UDI
- Commercial Distribution
- Not 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
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
Moist Heat or Steam Sterilization FDA UDI
Snowden-Pencer by Carefusion 2200, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Carefusion 2200, Inc
Sources (1)
- FDA UDI f84795dc-34e3-48a2-84e2-1a9ccaf8ee74 36 fields · synced Jun 6, 2026