Identity
- Trade Name
- AROSurgical Artery Vascular Clamp FDA UDI
- Generic Name
- Suturing needle, single-use FDA UDI
- Device Name
- End to Side Clamps, 1/2" Radius, Blue, 50g, Box/10 FDA UDI
- Model / Reference
- HK-2 FDA UDI
- Description
- End to Side Clamps, 1/2" Radius, Blue, 50g, Box/10 FDA UDI
Identifiers
- Catalog Number
- HK-2 FDA UDI
- Primary DI / UDI-DI
- 10818245020212 FDA UDI
- FDA Product Code
- GAR FDA UDI
- GMDN Term
- Suturing needle, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.5020 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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 22.5 Millimeter FDA UDI
Category: Suturing needle, single-use
AROSurgical Artery Vascular Clamp by Aros Surgical Instruments Corporation — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Aros Surgical Instruments Corporation
Sources (1)
- FDA UDI 372328b6-43f4-452b-8194-9d28fe9d3cf6 36 fields · synced May 30, 2026