Identity
- Trade Name
- BloodSTOP iX Trauma Matrix FDA UDI
- Generic Name
- Plant polysaccharide haemostatic agent, non-bioabsorbable, non-antimicrobial FDA UDI
- Device Name
- BloodSTOP IX Hemostat Trauma Care Matrix 12"X12" (30cmX30cm) FDA UDI
- Model / Reference
- BM-iX-25 FDA UDI
- Description
- BloodSTOP IX Hemostat Trauma Care Matrix 12"X12" (30cmX30cm) FDA UDI
Identifiers
- Catalog Number
- BM-iX-25 FDA UDI
- Primary DI / UDI-DI
- 00850744001586 FDA UDI
- FDA Product Code
- FRO FDA UDI
- GMDN Term
- Plant polysaccharide haemostatic agent, non-bioabsorbable, non-antimicrobial FDA UDI
Classification
- Device Class
- U 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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Area/Surface Area — 144 Square inch FDA UDI
Category: Plant polysaccharide haemostatic agent, non-bioabsorbable, non-antimicrobial
BloodSTOP iX Trauma Matrix by LifeScience PLUS, Inc. — Class U — 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 U | Pending data |
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Manufacturer
- Manufacturer
- LifeScience PLUS, Inc.
Sources (1)
- FDA UDI e832ca9b-39e9-4aa2-9ddd-d9153160cf30 36 fields · synced Jun 9, 2026