Identity
- Trade Name
- TZ Medical Pressure Discs FDA UDI
- Generic Name
- Femoral artery compression system, manual, single-use FDA UDI
- Device Name
- Round Universal Disc FDA UDI
- Model / Reference
- 8880-02 FDA UDI
- Description
- Round Universal Disc FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00811331010053 FDA UDI
- 510(k) Number
- K914149 FDA UDI
- FDA Product Code
- DXC FDA UDI
- GMDN Term
- Femoral artery compression system, manual, single-use FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.4450 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
No
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 system, manual, single-use
TZ Medical Pressure Discs by Tz Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Femoral artery compression system, manual, single-use.
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- ComfortPress Hand-Held Vascular Compression Assist Device — Semler Technologies, Inc. · Class II
- ComfortPress Hand-Held Vascular Compression Assist Device — Semler Technologies, Inc. · Class II
- SAFEGUARD® — Merit Medical Systems, Inc. · Class II
- SAFEGUARD™ — Merit Medical Systems, Inc. · Class II
Cleared under the same submission
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 II | Pending data |
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Manufacturer
- Manufacturer
- Tz Medical, Inc.
Sources (1)
- FDA UDI 0a9d60a8-d015-45e4-af6f-fd1c61e79922 34 fields · synced May 31, 2026