Identity
- Trade Name
- AESCULAP FDA UDI
- Generic Name
- Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
- Device Name
- MIASPAS MINI-TTA Lung Retractor Blade, M, depth: 140 mm, width: 35 mm, titanium, with ball snap closure, non-sterile, reusable FDA UDI
- Model / Reference
- BV165T FDA UDI
- Description
- MIASPAS MINI-TTA Lung Retractor Blade, M, depth: 140 mm, width: 35 mm, titanium, with ball snap closure, non-sterile, reusable FDA UDI
Identifiers
- Catalog Number
- BV165T FDA UDI
- Primary DI / UDI-DI
- 04038653199761 FDA UDI
- FDA Product Code
- HRX FDA UDI
- GMDN Term
- Orthopaedic prosthesis implantation positioning instrument, reusable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.1100 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
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
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Aesculap by Aesculap, Inc. — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Aesculap, Inc.
Sources (1)
- FDA UDI 32c07e86-0c5f-4557-9475-f0e0b32616ab 36 fields · synced Jun 1, 2026