Identity
- Trade Name
- Instrapac FDA UDI
- Generic Name
- Podiatric probe, single-use FDA UDI
- Device Name
- Instrapac Swan Neck Probe 12cm X 50 FDA UDI
- Model / Reference
- 8280 FDA UDI
- Description
- Instrapac Swan Neck Probe 12cm X 50 FDA UDI
Identifiers
- Catalog Number
- 8280 FDA UDI
- Primary DI / UDI-DI
- 05010058082809 FDA UDI
- FDA Product Code
- HXB FDA UDI
- GMDN Term
- Podiatric probe, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.4540 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
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
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Length — 12 Centimeter FDA UDI
Category: Podiatric probe, single-use
Instrapac by Robinson Healthcare Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Podiatric probe, single-use.
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
- Robinson Healthcare Limited
Sources (1)
- FDA UDI 265274ff-3838-458a-804b-77d5aaee857a 37 fields · synced May 30, 2026