SCANLAN® Needle Holders 3003-229
by Scanlan International Inc EUDAMEDGUDID
Active
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing GUDID | Number00846159003031 | Date23 May 2016 | StatusIn distribution |
| European Union | CE/MDD EUDAMED | Number— | Date— | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
- European Union
- United States
Recalls
No FDA recalls on record, checked 23 Oct 2026.
Specification
- Trade Name
- SCANLAN® Needle HoldersJacobson Micro Needle HolderJacobson Micro Needle Holder Diamond Dust™ jawSCANLAN® Microsurgical InstrumentsJacobson Micro Needle Holder Round HandleJacobson Micro Needle Holder Flat HandleJacobson Micro Needle Holder Flat Knurled HandleSCANLAN® Dilators
- Generic Name
- Suturing needle holder, reusableOpen-surgery dissectorVascular dilator, reusableNeurosurgical probe
- Model / Ref / Catalog
- 3003-229, 6006-120M, 6006-177, 3781-10, 6006-124, 6006-131, 6006-176, 3003-261, 3003-202, 6006-126, 6006-123, 6006-160, 6006-127, Q31088-6, 6006-102, 3003-224, 3003-241, 3003-235, 3003-187, 6006-173, 6006-122, 3003-206-12, 3003-234, 3003-200-12, 6006-159, 6006-108, 6006-125, 3003-240, 3003-237, 3003-183, 8008-480, 3003-176, 3784-31, 6006-96, 3003-204-12, 6006-17, 8008-460, 3003-263, 3003-228, 3003-193, 3003-171, 3003-175, 6006-92, 6006-130, 6006-170, 6006-80, 3003-197, 6006-82, 6006-100, 6006-84, 3003-194
- Primary DI / UDI-DI
- 00846159003031, 00846159020427, 00846159023305, 00846159032659, 00846159004854, 00846159004915, 00846159020496, 00846159003116, 00846159002966, 00846159020434, 00846159004847, 00846159004991, 00846159004878, 00846159025200, 00846159004762, 00846159002997, 00846159019209, 00846159003062, 00846159015010, 00846159023299, 00846159004830, 00846159019094, 00846159003048, 00846159002959, 00846159004984, 00846159004786, 00846159004861, 00846159019193, 00846159003086, 00846159002874, 00846159025118, 00846159018974, 00846159003994, 00846159026917, 00846159019070, 00846159004434, 00846159024999, 00846159003123, 00846159019148, 00846159002928, 00846159008708, 00846159008746, 00846159004731, 00846159004908, 00846159005004, 00846159026900, 00846159019056, 00846159004687, 00846159004755, 00846159004694, 00846159019032
- FDA Product Code
- FHQ, GDI, DWP, GZX
- GMDN Term
- Suturing needle holder, reusableOpen-surgery dissectorVascular dilator, reusableNeurosurgical probe
- Device Class
- Class IClass II
- Regulation Number
- 876.4730, 878.4800, 870.4475, 882.4525
- Commercial Distribution
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from Scanlan International Inc
Properties
Other properties (11)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Expiration Date: No
- Manufacturing Date: No