DRAP REGISTERED MEDICAL DEVICE
Neodent (GM Micro Abutment) is registered with DRAP under number MDIR-0008503 as a Class C (moderate to high risk) medical device, imported. The listed holder is Stupra International. It is listed as valid until 25 Mar 2030.
Screening result
i
Number type: imported, registered (Class B, C or D)
MDIR-0008503
MDIR-0008503
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Found in DRAP's published list
DRAP registered Class B/C/D list, 28 Aug 2025
DRAP registered Class B/C/D list, 28 Aug 2025
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Listed valid until 25 Mar 2030
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Holder has a DRAP import licence on file
ELI-00953
ELI-00953
| Device | Neodent (GM Micro Abutment) |
|---|---|
| Class | C |
| Listed holder | Stupra International |
| Holder address | 289-A, Muslim Town Lahore |
| Manufacturing site | M/s Institute Straumann AG Peter Merian-Weg 12 4002 Basel, Switzerland. M/s JJGC Industria e Comericio de Materialis Dentarios S. A Av. Juscelino Kubitschek de Oliveira 3291-CIC Curitiba Parana BR Postal code 81270-4000 |
| Issued | 26 Mar 2025 |
| Renewal date | 25 Mar 2030 |
| Licence | ELI-00953 |
Specifications
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Screened 5 Oct 2026, 00:52 (Pakistan time). A screening aid, not an official DRAP verification.
More devices from this holder
Other DRAP registrations and enlistments listed for the same company.
| MDIR-0007178 | Straumann (Bone Level Tapered Implant) | Class C |
| MDIR-0007179 | Straumann (Cementable Abutment) | Class C |
| MDIR-0007180 | Straumann (Bone Level Implant) | Class C |
| MDIR-0007181 | Straumann (Screw-Retained Abutment) | Class C |
| MDIR-0007182 | Straumann (Standard Plus Implant) | Class C |
| MDIR-0007183 | Straumann (Healing Abutment) | Class C |
| MDIR-0008500 | Neodent GM Cover Screw | Class C |
| MDIR-0008501 | Neodent (GM Healing Abutment) | Class C |
| MDIR-0008502 | Neodent (GM Mini Conical Abutment) | Class C |
| MDIR-0008504 | Neodent (GM Helix Acqua Implant) | Class C |
| MDIR-0008505 | Neodent (GM Helix Implant) | Class C |
| MDIR-0008506 | Neodent GM Exact Click Universal Abutment 17/30 | Class C |
Corrections
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Source: DRAP's published provisional lists. A screening aid, not an official DRAP verification; confirm with DRAP and the supplier's original documents.