Super Bypass SB-1207
Super Bypass SB-1207 is a Class I device made by Takayama Instruments Inc., listed in FDA GUDID since 26 Jun 2025 (UDI-DI 04580036673202), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04580036673202 | Date26 Jun 2025 | StatusListed |
Official records
- AccessGUDID record 04580036673202
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Super Bypass
- Generic name
- Surgical soft-tissue manipulation forceps, tweezers-like, reusable
- Model / Ref / Catalog
- SB-1207
- Primary DI / UDI-DI
- 04580036673202
- FDA product code
- GEN
- GMDN term
- Surgical soft-tissue manipulation forceps, tweezers-like, reusable
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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