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Shifeng
FDA UDIClass II (US FDA UDI)
by Chengdu Xinjin Shifeng Medical Apparatus & Instrument Co., Ltd.
Identity
- Trade Name
- Shifeng FDA UDI
- Generic Name
- Anaesthesia Luer syringe FDA UDI
- Model / Reference
- S-3000 FDA UDI
Identifiers
- Primary DI / UDI-DI
- G001S30000 FDA UDI
- FDA Product Code
- FMF FDA UDI
- GMDN Term
- Anaesthesia Luer syringe FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5860 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
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Anaesthesia Luer syringe
Shifeng by Chengdu Xinjin Shifeng Medical Apparatus & Instrument Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Anaesthesia Luer syringe.
- Syringe 3ml — GERI-GENTLE CORPORATION · Class II
- Shifeng — Chengdu Xinjin Shifeng Medical Apparatus & Instrument Co., Ltd. · 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
Sources (1)
- FDA UDI a5b7c425-8f28-4757-8db4-6e25c49ebf80 32 fields · synced May 30, 2026