GRYPHON P PEEK DS ANCHOR w/ DYNACORD
EUDAMEDFDA UDIClass IIb (EU MDR)
Identity
- Trade Name
- GRYPHON P PEEK DS ANCHOR w/ DYNACORD EUDAMEDGRYPHON DYNACORD FDA UDI
- Generic Name
- Tendon/ligament bone anchor, non-bioabsorbable FDA UDI
- Device Name
- GRYPHON PEEK Anchor, DYNACORD Suture, Blue, White/Blue/Green Striped EUDAMEDGRYPHON P PEEK DS ANCHOR w/DYNACORD PEEK Anchor (1) Blue (1) White/Blue/Green Striped, Size 2 (5 Metric) DYNACORD Suture, 36 inches (91cm) FDA UDI
- Model / Reference
- GRYPHON PEEK DYNACORD EUDAMED210123 EUDAMEDFDA UDI
- Description
- GRYPHON P PEEK DS ANCHOR w/DYNACORD PEEK Anchor (1) Blue (1) White/Blue/Green Striped, Size 2 (5 Metric) DYNACORD Suture, 36 inches (91cm) FDA UDI
Identifiers
- Catalog Number
- 210123 FDA UDI
- Primary DI / UDI-DI
- 10886705029907 EUDAMEDFDA UDI
- Basic UDI-DI
- 0886705a00082KK EUDAMED
- 510(k) Number
- K181809 FDA UDI
- FDA Product Code
- MBI FDA UDI
- EMDN Code
- P09120102 ANCHORS, TENDON AND LIGAMENT SYNTHESIS EUDAMED
- GMDN Term
- Tendon/ligament bone anchor, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 888.3040 FDA UDI
- Market of Registration
- Belgium EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
Single Use
Yes
Implantable
Yes
Reusable
No
Contains Latex
No
Reprocessed
No
Sutures
Yes
CMR Substance
Yes
Human-derived
No
Human Tissues
No
Animal Tissues
No
Endocrine Disruptor
No
Administering Medicine
No
Measuring Function
No
Incorporates Medicinal Product
No
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
No
Lot / Batch Number
Yes
Serial Number
No
Expiration Date
Yes
Manufacturing Date
No
Category: Hand-held surgical retractor, reusable
GRYPHON P PEEK DS ANCHOR w/ DYNACORD by Medos International Sarl — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
CE/MDR
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 0886705a00082KK | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
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Manufacturer
- Manufacturer
- Medos International SARL
- EUDAMED SRN
- CH-MF-000014268
- Authorised Representative
- DePuy Ireland UC IE-AR-000009328
Sources (2)
- EUDAMED a0820669-1d75-4d73-bbc3-1eebc6986843 61 fields · synced Jun 19, 2026
- FDA UDI 7ac0efcd-8d0a-4542-8d02-518b2f05b9f1 36 fields · synced May 30, 2026