Identity
- Trade Name
- VanishPoint Syringe EUDAMEDVanishPoint® FDA UDI
- Generic Name
- Metered-delivery hypodermic syringe/needle FDA UDI
- Device Name
- VanishPoint Syringe EUDAMED1mL 25G x 1" VanishPoint® Syringe FDA UDI
- Model / Reference
- 10161 EUDAMEDFDA UDI
- Description
- 1mL 25G x 1" VanishPoint® Syringe FDA UDI
Identifiers
- Catalog Number
- 10161 FDA UDI
- Primary DI / UDI-DI
- 00613703101600 EUDAMEDFDA UDI
- Basic UDI-DI
- 0613703VPsyringeF9 EUDAMED
- 510(k) Number
- K980069 FDA UDI
- FDA Product Code
- MEG FDA UDI
- EMDN Code
- A02010205 INFUSION AND IRRIGATION SYRINGES WITH SAFETY SYSTEM, SINGLE-USE EUDAMED
- GMDN Term
- Metered-delivery hypodermic syringe/needle FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 880.5860 FDA UDI
- Market of Registration
- Germany 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
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
Yes
EUDAMED
Measuring Function
Yes
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
Yes
FDA UDI
VanishPoint Syringe by Retractable Technologies, Inc. — Class IIa — FDA_510K, MDR — listed in EUDAMED, FDA GUDID, FDA 510(k) — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
United States Active
FDA_510K
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K980069 | Class IIa | Active |
| EUDAMED | European Union | CE/MDR | 0613703VPsyringeF9 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Retractable Technologies, Inc.
- EUDAMED SRN
- US-MF-000031781
- Authorised Representative
- MDSS GmbH DE-AR-000005430
Sources (3)
- EUDAMED 3b6e015f-6292-4850-bf78-93065e63fe36 61 fields · synced Jul 9, 2026
- FDA UDI 43fd87e1-93a3-4b48-9667-3669c0e21973 36 fields · synced May 30, 2026
- FDA 510(k) K980069 1 fields · synced May 18, 2026