Identity
- Trade Name
- MyoSure Single Use Seal EUDAMEDMyoSure Tissue Removal Device FDA UDI
- Generic Name
- Endoscope working-channel seal FDA UDI
- Device Name
- Omni Lok Cervical Seal; Omni 5Fr Seal Cap; MyoSure Single Use Seal EUDAMEDMyoSure Single Use Seals are an accessory to the Hologic Hysteroscopes and are used to prevent distension fluid leakage from the proximal ends of hysteroscope and removable outflow channel. FDA UDI
- Model / Reference
- 40-902 EUDAMEDFDA UDI
- Description
- MyoSure Single Use Seals are an accessory to the Hologic Hysteroscopes and are used to prevent distension fluid leakage from the proximal ends of hysteroscope and removable outflow channel. FDA UDI
Identifiers
- Catalog Number
- 40-902 FDA UDI
- Primary DI / UDI-DI
- 25420045505107 EUDAMEDFDA UDI
- Basic UDI-DI
- 54200455GSSSCOPESEALWP EUDAMED
- Unit of Use DI
- 15420045505100 EUDAMED
- 510(k) Number
- K142029 FDA UDI
- FDA Product Code
- HIH FDA UDI
- EMDN Code
- Z12020785 GENITOURINARY ENDOSCOPY INSTRUMENTS - CONSUMABLES EUDAMED
- GMDN Term
- Endoscope working-channel seal FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 884.1690 FDA UDI
- Market of Registration
- Belgium EUDAMED
- 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
Yes
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
No
FDA UDI
MyoSure Single Use Seal by Hologic Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
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 | 54200455GSSSCOPESEALWP | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Hologic, Inc.
- EUDAMED SRN
- US-MF-000003310
- Authorised Representative
- Hologic BV BE-AR-000000127
Sources (2)
- EUDAMED d9542a5e-494b-4ab4-9d7b-16eaf64d99e0 61 fields · synced Jun 19, 2026
- FDA UDI d411ccd1-0b5a-4820-9881-431be3c8f594 35 fields · synced May 30, 2026