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Global Apg+
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 2230-00-029Model Drilling Power Tool Attachment, BasicRef 2236-26-000Model Hand-Held Surgical Retractor, Reusable
Identity
- Trade Name
- GLOBAL APG+ EUDAMEDFDA UDIGLOBAL EUDAMEDFDA UDI
- Generic Name
- Hand-held surgical retractor, reusable FDA UDIDrilling power tool attachment, basic FDA UDI
- Device Name
- Drilling Power Tool Attachment, Basic EUDAMEDHand-Held Surgical Retractor, Reusable EUDAMEDGLOBAL MODF CREGO RETRACTOR FDA UDIGLOBAL APG+ QUICK CONNECT DRIVER SHAFT FDA UDI
- Model / Reference
- Drilling Power Tool Attachment, Basic EUDAMED2230-00-029 EUDAMEDFDA UDI2236-26-000 EUDAMEDFDA UDIHand-Held Surgical Retractor, Reusable EUDAMED
- Description
- GLOBAL MODF CREGO RETRACTOR FDA UDIGLOBAL APG+ QUICK CONNECT DRIVER SHAFT FDA UDI
Identifiers
- Catalog Number
- 223626000 FDA UDI223000029 FDA UDI
- Primary DI / UDI-DI
- 10603295103028 EUDAMEDFDA UDI10603295106142 EUDAMEDFDA UDI
- Basic UDI-DI
- 0603295a0053592 EUDAMED0603295a004168R EUDAMED
- Direct Marketing DI
- 10603295103028 EUDAMED10603295106142 EUDAMED
- FDA Product Code
- GAD FDA UDIHWR FDA UDI
- EMDN Code
- L090999 ORTHOPAEDIC SURGERY CUTTING INSTRUMENTS, REUSABLE - OTHER EUDAMEDL0915 SPREADERS AND RETRACTORS FOR ORTHOPAEDIC SURGERY, REUSABLE EUDAMED
- GMDN Term
- Hand-held surgical retractor, reusable FDA UDIDrilling power tool attachment, basic FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I EUDAMEDFDA UDI
- Regulation Number
- 878.4800 FDA UDI888.4540 FDA UDI
- Market of Registration
- Ireland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMEDEUDAMED
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
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
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: Bone cutting forceps, reusable
Global Apg+ by DePuy Ireland UC — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 0603295a0053592 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- DePuy Ireland UC
- EUDAMED SRN
- IE-MF-000007377
Sources (4)
- EUDAMED d98ba3fc-dca8-4aca-ac14-ec068b86c3b6 61 fields · synced Jul 12, 2026
- FDA UDI 4f706998-0e15-461d-9482-b1161a56ee37 35 fields · synced May 30, 2026
- FDA UDI e5d4a6cc-c8ef-4db0-89f3-15800bc10916 35 fields · synced May 30, 2026
- EUDAMED a9a5755f-1ef8-4377-8597-f2aee931ca10 61 fields · synced Jun 20, 2026