Identity
- Trade Name
- Segment Sampler (SEG) FDA UDI
- Generic Name
- Blood donor bag segment sampling IVD FDA UDI
- Device Name
- SEG is intended to aid extraction of a biological fluid sample from a segmented piece of tubing. FDA UDI
- Model / Reference
- A200200 FDA UDI
- Description
- SEG is intended to aid extraction of a biological fluid sample from a segmented piece of tubing. FDA UDI
Identifiers
- Catalog Number
- A200200 FDA UDI
- Primary DI / UDI-DI
- 19555240401332 FDA UDI
- FDA Product Code
- KSS FDA UDI
- GMDN Term
- Blood donor bag segment sampling IVD FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 864.9050 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
Yes
FDA UDI
Segment Sampler (SEG) by Itl Asia Pacific Sdn. Bhd. — Class I — 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 I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Itl Asia Pacific Sdn. Bhd.
Sources (1)
- FDA UDI 2a6159a5-7a4a-4ea8-ab8f-0fd01b1b9665 38 fields · synced Jun 8, 2026