Mk-700700-40
Mk-700700-40 is a Class I device made by Microspecialities, Inc., listed in FDA GUDID since 3 Jan 2019 (UDI-DI 10810003222371), 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 | Number10810003222371 | Date3 Jan 2019 | StatusListed |
Official records
- AccessGUDID record 10810003222371
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Keratome blade, single-use
- Model / Ref / Catalog
- MK-700700-40
- Description
- MicroKeratome Blades, MORIA M2 minus 40. Have the ultimate control of corneal flap thickness while using a single head. Range from -40 to +20 microns. 10/bx
- Primary DI / UDI-DI
- 10810003222371
- FDA product code
- HNO
- GMDN term
- Keratome blade, single-use
- Device class
- Class I
- Regulation number
- 886.4370
- GUDID distribution status
- In Commercial Distribution
- Size
- Angle — -40 degree
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