Identity
- Trade Name
- STILLE Retractors FDA UDI
- Generic Name
- Nerve/vessel retractor FDA UDI
- Device Name
- NERVE RETRACTOR LOVE STILLE 7 mm 20.5 cm 8 in FDA UDI
- Model / Reference
- 108-26048-7 FDA UDI
- Description
- NERVE RETRACTOR LOVE STILLE 7 mm 20.5 cm 8 in FDA UDI
Identifiers
- Catalog Number
- 108-26048-7 FDA UDI
- Primary DI / UDI-DI
- 07332339212209 FDA UDI
- FDA Product Code
- HAO FDA UDI
- GMDN Term
- Nerve/vessel retractor FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 882.4535 FDA UDI
- Commercial Distribution
- 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
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
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Length — 20.5 Centimeter FDA UDI
Category: Nerve/vessel retractor
STILLE Retractors by Stille AB — 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
- Stille AB
Sources (1)
- FDA UDI 6b0efda4-66d6-4407-bbbf-687475df35f5 36 fields · synced Jun 8, 2026