Absorbent Paper Points, NC 45 2584
Model 45
Absorbent Paper Points, NC 45 2584 is an endodontic paper point (EU MDD Class IIa; FDA Class I; FDA product code EKN, Point, Paper, Endodontic) made by Meta Biomed Co., Ltd., registered in EUDAMED on 24 Jun 2026 (Basic UDI-DI B-08806387825845) and listed in FDA GUDID since 24 Sep 2022 (UDI-DI 08806387825845), active as of 12 Nov 2026.
Active
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-08806387825845 08806387825845 | Date24 Jun 2026 | StatusActive |
| United States | GUDID listing GUDID | Number08806387825845 | Date24 Sep 2022 | StatusListed |
Official records
- EUDAMED public site B-08806387825845
- AccessGUDID record 08806387825845
Across registries
- EUDAMED Basic UDI-DI B-08806387825845 registered 24 Jun 2026 Active
- FDA GUDID UDI-DI 08806387825845 listed 24 Sep 2022 Listed
Timeline
- Listed FDA GUDID 08806387825845
- Registered EUDAMED B-08806387825845
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Absorbent Paper Points EUDAMEDAbsorbent Paper Points, NC 45 GUDID
- Generic name
- Endodontic paper point
- Device name
- Sterile Absorbent Paper Points
- Model / reference
- 45 EUDAMED2584 GUDID
- Primary DI / UDI-DI
- 08806387825845
- Basic UDI-DI
- B-08806387825845
- FDA product code
- EKN
- EMDN code
- Q01010401 Paper and gutta-percha tips, matrices and wedges for dentistry
- GMDN term
- Endodontic paper point
- Device class
- Class IIa EUDAMEDClass I GUDID
- Regulation number
- 872.3830
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Radiation Sterilization
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 45 | 2584 |
| Device class | Class IIa | Class I |
| Sterilise before use | No | Yes |
Registry differences
EUDAMED and FDA GUDID describe the same product (same UDI-DI) and state different values:
- Sterilise before use UDI-DI 08806387825845: EUDAMED states No, FDA GUDID states Yes.
Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.
Similar devices in this category
Other devices filed under PAPER AND GUTTA-PERCHA TIPS, MATRICES AND WEDGES FOR DENTISTRY.
- MM MARKED PAPER POINTS DIA-PROISO-.06 PLUS 15 MP259-S603 by DiaDent Group International
- ABSORBENT PAPER POINTS DIA-SYSTEM GTP.08 20 242-608 by DiaDent Group International
- myQuickmat All-round introkit 6850 by Polydentia SA
- myQuickmat Prime kit 6890 by Polydentia SA
- Omni-Matrix Original 2201 by ULTRADENT PRODUCTS, INC.