Identity
- Trade Name
- E-LINE FDA UDI
- Generic Name
- Rigid endoscope obturator FDA UDI
- Device Name
- OBTURATOR FOR CYSTOSCOPE 21FR color code blue, WL 230mm, oval, rounded distal end, compatible with sheath 86520446, reusable FDA UDI
- Model / Reference
- 86520447 FDA UDI
- Description
- OBTURATOR FOR CYSTOSCOPE 21FR color code blue, WL 230mm, oval, rounded distal end, compatible with sheath 86520446, reusable FDA UDI
Identifiers
- Catalog Number
- 8652.0447 FDA UDI
- Primary DI / UDI-DI
- 04055207045572 FDA UDI
- FDA Product Code
- FBO FDA UDI
- GMDN Term
- Rigid endoscope obturator FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.1500 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
No
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
- Outer Diameter — 7 Millimeter FDA UDI
Category: Rigid endoscope obturator
E-Line by Richard Wolf GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Rigid endoscope obturator.
- Arthroscopy bridge — SOPRO-COMEG GmbH · Class II
- Biportal Laminoscope, ocular — Joimax GmbH · Class IIa
- TAUT — TELEFLEX INCORPORATED · Class II
- Hysteroscopy obturator — SOPRO-COMEG GmbH · Class II
- USA Elite — Gyrus Acmi, Inc. · Class II
- Trabecular Metal® — Zimmer, Inc. · Class I
- Obturator — SOPRO-COMEG GmbH · Class II
- Obturator — SOPRO-COMEG GmbH · 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 II | Pending data |
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Manufacturer
- Manufacturer
- Richard Wolf GmbH
Sources (1)
- FDA UDI d3b9c4dd-b5fd-49df-9ebb-3fd6751ba42b 36 fields · synced Jun 8, 2026