Identity
- Trade Name
- Laryngeal mirror, rhodium coated FDA UDI
- Generic Name
- Laryngeal mirror, reusable FDA UDI
- Device Name
- without handle, without screw size 9, 28 mm FDA UDI
- Model / Reference
- 40-524-09 FDA UDI
- Description
- without handle, without screw size 9, 28 mm FDA UDI
Identifiers
- Catalog Number
- 40-524-09 FDA UDI
- Primary DI / UDI-DI
- 04250381889145 FDA UDI
- FDA Product Code
- LRC FDA UDI
- GMDN Term
- Laryngeal mirror, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 874.4420 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
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
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
Category: Laryngeal mirror, reusable
Laryngeal mirror, rhodium coated by Spiggle & Theis Medizintechnik GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Laryngeal mirror, reusable.
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- Hahnenkratt — E. Hahnenkratt GmbH · Class I
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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
- Spiggle & Theis Medizintechnik GmbH
Sources (1)
- FDA UDI d5da3fcd-78d0-4bd3-904f-c9b0217d8887 35 fields · synced Jun 8, 2026