Identity
- Trade Name
- StecoGuide FDA UDI
- Generic Name
- Surgical drill guide, single-use FDA UDI
- Device Name
- Titanium single sleeve D3.0/d2.35/L5 for implant planning and CT analysis -> For further information visit steco.de FDA UDI
- Model / Reference
- M.27.01.D235L5 FDA UDI
- Description
- Titanium single sleeve D3.0/d2.35/L5 for implant planning and CT analysis -> For further information visit steco.de FDA UDI
Identifiers
- Catalog Number
- M.27.01.D235L5 FDA UDI
- Primary DI / UDI-DI
- ESTOM2701D235L50 FDA UDI
- FDA Product Code
- NDP FDA UDI
- GMDN Term
- Surgical drill guide, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.3980 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Surgical drill guide, single-use
StecoGuide by steco-System-Technik GmbH & Co KG — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- steco-System-Technik GmbH & Co KG
Sources (1)
- FDA UDI 2cde2581-e65c-4a4c-a55a-a6db66851d01 35 fields · synced May 30, 2026