Identity
- Trade Name
- Tech-Med FDA UDI
- Generic Name
- Blood pressure cuff, reusable FDA UDI
- Device Name
- BP Kit, 22"Sprague, Light Blue FDA UDI
- Model / Reference
- 2080LB FDA UDI
- Description
- BP Kit, 22"Sprague, Light Blue FDA UDI
Identifiers
- Catalog Number
- 2080LB FDA UDI
- Primary DI / UDI-DI
- 00665973016887 FDA UDI
- 510(k) Number
- K780715 FDA UDI
- FDA Product Code
- DXQ FDA UDI
- GMDN Term
- Blood pressure cuff, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1120 FDA UDI
- Commercial Distribution
- Not 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
Yes
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Weight — 0.8 Kilogram FDA UDI
Tech-Med by Dukal LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K780715 also covers:
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
- Dukal LLC
Sources (1)
- FDA UDI 4a0739b2-3669-4fd8-905c-5dd79244e66f 38 fields · synced Jun 1, 2026