Cyotplast™ RTMTape RTMTAPE10
by Osteogenics Biomedical, Inc.
Ref RTMTAPE10
Cyotplast™ RTMTape RTMTAPE10 is a device classified as Class III (EU), Unclassified (US) made by Osteogenics Biomedical, Inc., registered in EUDAMED on 25 Jun 2026 (Basic UDI-DI B-D765RTMTAPE100) and listed in FDA GUDID since 9 Dec 2016 (UDI-DI D765RTMTAPE100), active as of 23 Oct 2026.
Active
CE MDD
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-D765RTMTAPE100 D765RTMTAPE100 | Date25 Jun 2026 | StatusActive |
| United States | GUDID listing GUDID | NumberD765RTMTAPE100 | Date9 Dec 2016 | StatusListed |
Official records
- EUDAMED public site B-D765RTMTAPE100
Across registries
- EUDAMED Basic UDI-DI B-D765RTMTAPE100 registered 25 Jun 2026 Active
- FDA GUDID UDI-DI D765RTMTAPE100 listed 9 Dec 2016 Listed
Timeline
- Listed FDA GUDID D765RTMTAPE100
- Registered EUDAMED B-D765RTMTAPE100
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Cytoplast RTM TAPE EUDAMEDCyotplast™ RTMTape GUDID
- Generic name
- General oral wound dressing, animal-derived
- Device name
- Bovine Dermis Collagen Dental Wound Dressings - Tape
- Model / reference
- RTMTAPE10
- Primary DI / UDI-DI
- D765RTMTAPE100
- Basic UDI-DI
- B-D765RTMTAPE100
- FDA product code
- KGN
- EMDN code
- Q010304 Periodontal dressings
- GMDN term
- General oral wound dressing, animal-derived
- Device class
- Class III EUDAMEDU GUDID
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Size
- Width — 2.5 CentimeterLength — 7.5 Centimeter
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class III | U |
| Implantable | Yes | No |
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