Identity
- Trade Name
- EXEL 50ML SYRINGE L-L EUDAMEDEXEL 50ML SYRINGE L-L, Bulk Sterile, No Print on the Barrel FDA UDI
- Generic Name
- General-purpose syringe, single-use FDA UDI
- Device Name
- Syringe Only EUDAMEDEXEL 50ML SYRINGE L-L, Bulk Sterile, No Print on the Barrel, 4 Sets of Double PE Bags per Carton, 100/Bag, 400/CRTN FDA UDI
- Model / Reference
- 26300BSNP EUDAMEDFDA UDI
- Description
- EXEL 50ML SYRINGE L-L, Bulk Sterile, No Print on the Barrel, 4 Sets of Double PE Bags per Carton, 100/Bag, 400/CRTN FDA UDI
Identifiers
- Catalog Number
- 26300BSNP FDA UDI
- Primary DI / UDI-DI
- 00020221363005 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00020221363005 EUDAMED
- 510(k) Number
- K861153 FDA UDI
- FDA Product Code
- FMF FDA UDI
- EMDN Code
- A020199 SYRINGES, SINGLE-USE - OTHER EUDAMED
- GMDN Term
- General-purpose syringe, single-use FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 880.5860 FDA UDI
- Market of Registration
- Netherlands EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Exel 50ml Syringe L-L by Exelint International, Co. — Class I — 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-00020221363005 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Exelint International, Co.
- EUDAMED SRN
- US-MF-000037396
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (2)
- EUDAMED 73890ff5-db61-43f8-b007-6aa562d2c3d5 61 fields · synced Jun 18, 2026
- FDA UDI 86aab808-c942-4de0-9362-bc6ec9e123f2 35 fields · synced May 30, 2026