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Gryphon
FDA UDIEUDAMEDClass I (US FDA UDI)
Ref 211041Model General Orthopedic Use Obturators
Identity
- Trade Name
- GRYPHON BLUNT OBTURATOR EUDAMEDGRYPHON FDA UDI
- Generic Name
- Surgical drill guide obturator FDA UDI
- Device Name
- Obturator, Clear Cannula, Blunt, Reusable, Cannulated, Bone Graft, Screw Guide, Introducer, GRYPHON EUDAMEDGRYPHON BLUNT OBTURATOR FDA UDI
- Model / Reference
- 211041 EUDAMEDFDA UDIGeneral Orthopedic Use Obturators EUDAMED
- Description
- GRYPHON BLUNT OBTURATOR FDA UDI
Identifiers
- Catalog Number
- 211041 FDA UDI
- Primary DI / UDI-DI
- 10886705001538 EUDAMEDFDA UDI
- Basic UDI-DI
- 0886705a00128KJ EUDAMED
- Direct Marketing DI
- 10886705001538 EUDAMED
- FDA Product Code
- LXH FDA UDI
- EMDN Code
- L0999 ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Surgical drill guide obturator FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 888.4540 FDA UDI
- Market of Registration
- Belgium EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
Yes
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Surgical drill guide obturator
Gryphon by Medos International Sàrl — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Surgical drill guide obturator.
- TRIGEN — Smith & Nephew, Inc. · Class I
- DARCO — WRIGHT MEDICAL TECHNOLOGY, INC. · Class I
- SMALL CANNULATED SCREWS — Smith & Nephew, Inc. · Class II
- JUGGERKNOT FLEX OBTURATOR — Biomet Orthopedics, Inc. · Class II
- NexFix — TORNIER, INC. · Class I
- AM — WRIGHT MEDICAL TECHNOLOGY, INC. · Class I
- Marina Medical — MARINA MEDICAL INSTRUMENTS, INC. · Class I
- NexFix — TORNIER, INC. · Class I
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Medos International Sàrl
Sources (2)
- FDA UDI 58ec44b4-e0bc-462b-9c39-a4a2e96d58a4 35 fields · synced Jun 19, 2026
- EUDAMED c9dac431-13eb-4087-84e4-d49458c307ca 61 fields · synced Jun 19, 2026