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IMPROSAFE Multi Sample Needle
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 598123380Model 20G × 1ʺ; 20G × 1 1/2ʺ; 21G × 1″; 21G × 1 1/2″; 22G × 1″; 22G × 1 1/2″; 23G × 1ʺ; 23G × 1 1/2ʺRef 598120380Ref 598123250Ref 598121380
Identity
- Trade Name
- IMPROSAFE Multi Sample Needle EUDAMEDIMPROSAFE® Multi Sample Needle FDA UDI
- Generic Name
- Blood collection tube holder/needle FDA UDI
- Device Name
- IMPROSAFE® Multi Sample Needle EUDAMED
- Model / Reference
- 20G × 1ʺ; 20G × 1 1/2ʺ; 21G × 1″; 21G × 1 1/2″; 22G × 1″; 22G × 1 1/2″; 23G × 1ʺ; 23G × 1 1/2ʺ EUDAMED598123380 EUDAMED598120380 EUDAMED598123250 EUDAMED598121380 EUDAMED21G×1 1/2” FDA UDI
Identifiers
- Catalog Number
- 598121380 FDA UDI
- Primary DI / UDI-DI
- 06974481831733 EUDAMED06974481831719 EUDAMED06974481831726 EUDAMED06974481831139 EUDAMEDFDA UDI
- Basic UDI-DI
- 697448183001002US EUDAMED
- 510(k) Number
- K153388 FDA UDI
- FDA Product Code
- FMI FDA UDI
- EMDN Code
- A010199 NEEDLES FOR INFUSION AND COLLECTION - OTHER EUDAMED
- GMDN Term
- Blood collection tube holder/needle FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 880.5570 FDA UDI
- 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
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
Yes
FDA UDI
IMPROSAFE Multi Sample Needle by Guangzhou Improve Medical Instruments Co., Ltd. — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID
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 | 697448183001002US | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Guangzhou Improve Medical Instruments Co., Ltd
- EUDAMED SRN
- CN-MF-000006536
- Authorised Representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Sources (5)
- EUDAMED 42efcc3f-206f-4f64-8552-e2474a97c33f 61 fields · synced Aug 1, 2026
- EUDAMED 37ffbaa4-a068-4e16-bb7d-0ab2aafe2feb 61 fields · synced May 18, 2026
- EUDAMED 95a85dd4-438c-44f4-94b3-0fd9f419a0b6 61 fields · synced May 19, 2026
- EUDAMED 03533784-c91f-4571-bb9d-afd02f3f3dd9 61 fields · synced May 19, 2026
- FDA UDI 233c2f87-e98d-44e9-9a34-a0ba50bb1abb 34 fields · synced May 30, 2026