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Gryphon X

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 210826Model General Orthopedic Use Aiming and Guiding InstrumentsRef 210824Ref 219102Model General Orthopedic Use Obturators

by Medos International Sàrl

Identity

Trade Name
GRYPHON EUDAMEDFDA UDI
GRYPHON X FDA UDI
Generic Name
Fluted surgical drill bit, single-use FDA UDI
Orthopaedic guidewire, reusable FDA UDI
Surgical drill guide obturator FDA UDI
Device Name
Guide, Sawtooth, Slotted, Fishmouth, Shark, Drill Guide, Guidewire, Round, Trocar, Conical, Tip, Rod, Femoral, Tibial, Skid, Aimer, Offset, Femoral, Sleeve Removal Tool, Switching Stick, Bone Graft, Clear Cannula, Cap EUDAMED
Obturator, Clear Cannula, Blunt, Reusable, Cannulated, Bone Graft, Screw Guide, Introducer, GRYPHON EUDAMED
GRYPHON X 2.5MM DRILL BIT FDA UDI
GRYPHON Slotted Sawtooth Guide FDA UDI
GRYPHON Slotted Fishmouth Guide FDA UDI
GRYPHON Cannulated Hip Obturator FDA UDI
Model / Reference
210824 EUDAMEDFDA UDI
210826 EUDAMEDFDA UDI
219102 EUDAMEDFDA UDI
General Orthopedic Use Aiming and Guiding Instruments EUDAMED
General Orthopedic Use Obturators EUDAMED
271073 FDA UDI
Description
GRYPHON X 2.5MM DRILL BIT FDA UDI
GRYPHON Slotted Sawtooth Guide FDA UDI
GRYPHON Slotted Fishmouth Guide FDA UDI
GRYPHON Cannulated Hip Obturator FDA UDI

Identifiers

Catalog Number
271073 FDA UDI
210824 FDA UDI
210826 FDA UDI
219102 FDA UDI
Primary DI / UDI-DI
10886705024063 EUDAMEDFDA UDI
10886705024131 EUDAMEDFDA UDI
10886705027576 EUDAMEDFDA UDI
10886705033232 FDA UDI
Basic UDI-DI
0886705a00120K2 EUDAMED
0886705a00128KJ EUDAMED
Direct Marketing DI
10886705024131 EUDAMED
10886705027576 EUDAMED
FDA Product Code
HTW FDA UDI
LXH FDA UDI
FZX FDA UDI
EMDN Code
Z12139099 VARIOUS ORTHOPAEDIC AND TRAUMATOLOGY INSTRUMENTS - OTHER EUDAMED
GMDN Term
Fluted surgical drill bit, single-use FDA UDI
Orthopaedic guidewire, reusable FDA UDI
Surgical drill guide obturator FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.4540 FDA UDI
878.4800 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Fluted surgical drill bit, single-use

Gryphon X by Medos International Sàrl — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Fluted surgical drill bit, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medos International Sàrl

Sources (7)

  • FDA UDI d0ca0892-20f5-4f04-a594-911be3421a5f 35 fields · synced Jul 19, 2026
  • FDA UDI e5cb3c34-612b-495d-9700-7e31ef25d4c4 35 fields · synced May 30, 2026
  • FDA UDI fcfaa56c-898c-4263-a454-67c525d5ad62 35 fields · synced May 30, 2026
  • FDA UDI 951b898b-451e-4407-8d1d-ac5d1a960b7f 35 fields · synced May 30, 2026
  • EUDAMED 7a345423-154c-4880-b480-89b43ba8d0df 61 fields · synced Jun 20, 2026
  • EUDAMED 3dc9047a-b773-4108-ae6d-bf796866842b 61 fields · synced Jul 8, 2026
  • EUDAMED 9162e776-6c8f-4917-ac9d-72cf325ce366 61 fields · synced Jul 19, 2026