Identity
- Trade Name
- HSW SOFT-JECT® FDA UDI
- Generic Name
- General-purpose syringe, single-use FDA UDI
- Device Name
- 50ML (60ML) HSW SOFT-JECT® PERFUSION AMBER AK 2,00X30MM / 14GX1 1/4 FDA UDI
- Model / Reference
- 8300030253 FDA UDI
- Description
- 50ML (60ML) HSW SOFT-JECT® PERFUSION AMBER AK 2,00X30MM / 14GX1 1/4 FDA UDI
Identifiers
- Catalog Number
- 8300030253 FDA UDI
- Primary DI / UDI-DI
- 04035873046509 FDA UDI
- FDA Product Code
- FMF FDA UDI
- GMDN Term
- General-purpose syringe, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5860 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Total Volume — 50 Milliliter FDA UDI
Hsw Soft-Ject® by Henke-Sass, Wolf GmbH — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Henke-Sass, Wolf GmbH
Sources (1)
- FDA UDI 73ceaac3-17f5-4462-ac45-f4ef693f8134 37 fields · synced Jun 1, 2026