Identity
- Trade Name
- DCI FDA UDI
- Generic Name
- Flexible intubation laryngoscope, fibreoptic FDA UDI
- Device Name
- DCI® BONFILS Intubation Endoscope 5,0x40 FDA UDI
- Model / Reference
- 10331BD1 FDA UDI
- Description
- DCI® BONFILS Intubation Endoscope 5,0x40 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04048551225127 FDA UDI
- FDA Product Code
- CAL FDA UDI
- GMDN Term
- Flexible intubation laryngoscope, fibreoptic FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5530 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Flexible intubation laryngoscope, fibreoptic
Dci by Karl Storz GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Flexible intubation laryngoscope, fibreoptic.
- TRACHEAL INTUBATION FIBERSCOPE — Olympus Medical Systems Corporation · Class II
- FIBER INTUBATION SCOPE — PENTAX of America, Inc. · Class I
- FIBER INTUBATION SCOPE — PENTAX of America, Inc. · Class I
- FIBER INTUBATION SCOPE — PENTAX of America, Inc. · Class I
- FIBER INTUBATION SCOPE — PENTAX of America, Inc. · Class I
- SOS Shikani Optical Stylet, Adult — CLARUS MEDICAL, LLC · Class II
- PocketScope, pocket endoscope — CLARUS MEDICAL, LLC · Class II
- TRACHEAL INTUBATION FIBERSCOPE — Olympus Medical Systems Corporation · Class II
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
- Karl Storz GmbH & Co. KG
Sources (1)
- FDA UDI 892d5476-dd1f-4add-8ebe-0ef07e7e4483 33 fields · synced May 31, 2026