Identity
- Trade Name
- PEAK MEDICAL FDA UDI
- Generic Name
- Medical tubing clip/clamp, temporary, non-calibrated, reusable FDA UDI
- Device Name
- MANIFOLD DUAL TUBE HOLDER, 0.196" THICK, ANODISED CLEAR ALUMINIUM, 1.25 inch HIGH FOR TUBING SIZES. 0.5 inch, 0.375 inch, 0.375 inch, 0.25 inch, 0.25 inch, 0.25 inch, 0.0625 inch. FDA UDI
- Model / Reference
- 3324-0125BC FDA UDI
- Description
- MANIFOLD DUAL TUBE HOLDER, 0.196" THICK, ANODISED CLEAR ALUMINIUM, 1.25 inch HIGH FOR TUBING SIZES. 0.5 inch, 0.375 inch, 0.375 inch, 0.25 inch, 0.25 inch, 0.25 inch, 0.0625 inch. FDA UDI
Identifiers
- Primary DI / UDI-DI
- G45333240125BC0 FDA UDI
- FDA Product Code
- HXD FDA UDI
- GMDN Term
- Medical tubing clip/clamp, temporary, non-calibrated, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4800 FDA UDI
- Commercial Distribution
- 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
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
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
Category: Medical tubing clip/clamp, temporary, non-calibrated, reusable
Peak Medical by PEAK MEDICAL Distribution Inc — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- PEAK MEDICAL Distribution Inc
Sources (1)
- FDA UDI 425b204c-e1ea-4c60-8a12-5501d306dd5e 33 fields · synced May 31, 2026