Identity
- Trade Name
- BLITZ EUDAMEDFDA UDI
- Generic Name
- Suturing unit, single-use FDA UDI
- Device Name
- Orthopedic, Non-active, Instrument, Suture Retriever EUDAMEDBLITZ SUTURE RETRIEVER, STRAIGHT FDA UDIBLITZ SUTURE RETRIEVER, RIGHT, 45° FDA UDI
- Model / Reference
- C6311 EUDAMEDFDA UDIC6111 EUDAMEDFDA UDI
- Description
- BLITZ SUTURE RETRIEVER, STRAIGHT FDA UDIBLITZ SUTURE RETRIEVER, RIGHT, 45° FDA UDI
Identifiers
- Catalog Number
- C6111 FDA UDIC6311 FDA UDI
- Primary DI / UDI-DI
- 10845854018491 EUDAMEDFDA UDI10845854017692 EUDAMEDFDA UDI
- Basic UDI-DI
- B-10845854018491 EUDAMEDB-10845854017692 EUDAMED
- FDA Product Code
- NBH FDA UDIMDM FDA UDI
- EMDN Code
- H900899 SINGLE-USE INSTRUMENTS FOR SUTURES - OTHER EUDAMED
- GMDN Term
- Suturing unit, single-use FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 888.1100 FDA UDI878.4800 FDA UDI
- Market of Registration
- Belgium EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
No
FDA UDIFDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Angle — 45 degree FDA UDI
Blitz by Conmed Corporation — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-10845854018491 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Conmed Corporation
- EUDAMED SRN
- US-MF-000012663
- Authorised Representative
- MDSS GmbH DE-AR-000005430
Sources (6)
- EUDAMED ae732c92-b7d1-4652-bf30-2cda5130142f 61 fields · synced Jul 23, 2026
- EUDAMED 9f019337-45f4-403a-aa60-33598f7c173b 61 fields · synced May 17, 2026
- FDA UDI f6469750-4166-453f-b488-5060484ceca6 35 fields · synced May 30, 2026
- FDA UDI e62cc7af-ca3f-4ee4-bd21-a33e29448bcf 36 fields · synced May 30, 2026
- EUDAMED 7481bdef-eae7-45f2-b0fc-7b256a62a6fc 61 fields · synced Jul 10, 2026
- EUDAMED eb118263-e3fb-4bea-9e58-5d98461db86d 61 fields · synced Jul 23, 2026