Identity
- Trade Name
- Mini Compression Bandage FDA UDI
- Generic Name
- Femoral artery compression bandage, single-use FDA UDI
- Device Name
- 1ea - sterile compression bandage w/ 4" x 6" pad and 34" elastic wrap FDA UDI
- Model / Reference
- 01 FDA UDI
- Description
- 1ea - sterile compression bandage w/ 4" x 6" pad and 34" elastic wrap FDA UDI
Identifiers
- Catalog Number
- HHMCB01 FDA UDI
- Primary DI / UDI-DI
- M689HHMCB01010 FDA UDI
- FDA Product Code
- FQM FDA UDI
- GMDN Term
- Femoral artery compression bandage, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 880.5075 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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Femoral artery compression bandage, single-use
Mini Compression Bandage by Safeguard Us Operating, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Femoral artery compression bandage, single-use.
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- H-Bandage Compression Dressing, Flat Fols — H & H Medical Corporation · Class I
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
- Safeguard Us Operating, Llc
Sources (1)
- FDA UDI f262e2a6-b8a3-4033-bd91-2f56e3651d75 35 fields · synced Jun 8, 2026