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Results for “Ambler Surgical MICS capsulorhexis forceps”

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Registry EUDAMED FDA 510(k) FDA PMA GUDID 29

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Risk class Class I 29 Class IIa Class IIb Class III Class II (US)

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Class A Class B Class C Class D IVD General IVD Annex II List A IVD Annex II List B IVD for self-testing Active implantable (AIMDD) Unclassified (FDA) Not classified (FDA)

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29 devices foundsorted by relevance

Device · Manufacturer · Authorizations

Ambler Surgical Tija-Akahoshi MICS capsulorhexis forceps

Ambler Surgical, LLC,FDA registration: United States Class I

None GUDID I
Ambler Surgical Akahoshi MICS capsulorhexis forceps UDI-DI 00190660038205

Ambler Surgical, LLC,FDA registration: United States Class I

None GUDID I
3 variants
- Ambler Surgical Akahoshi MICS capsulorhexis forceps 9405E
- Ambler Surgical Akahoshi MICS capsulorhexis forceps 9406E
Ambler Surgical Giannetti MICS capsulorhexis forceps UDI-DI 00190660053895

Ambler Surgical, LLC,FDA registration: United States Class I

None GUDID I
4 variants
- Ambler Surgical Giannetti MICS capsulorhexis forceps 9440E
- See all variants of this device
Ambler Surgical Utrata MICS capsulorhexis forceps UDI-DI 00190660076696

Ambler Surgical, LLC,FDA registration: United States Class I

None GUDID I
7 variants
Ambler Surgical MICS capsulorhexis forceps UDI-DI 00190660065959

Ambler Surgical, LLC,FDA registration: United States Class I

None GUDID I
3 variants
- Ambler Surgical MICS capsulorhexis forceps 9908T
- Ambler Surgical MICS capsulorhexis forceps 9909T
Ambler Surgical Ambler MICS capsulorhexis forceps UDI-DI 00190660039325

Ambler Surgical, LLC,FDA registration: United States Class I

None GUDID I
5 variants
Ambler Surgical MICS capsulorhexis forceps tip UDI-DI 00190660065942

Ambler Surgical, LLC,FDA registration: United States Class I

None GUDID I
3 variants
- Ambler Surgical MICS capsulorhexis forceps tip 9918T
- See all variants of this device
Ambler Surgical Devgan MICS capsulorhexis forceps

Ambler Surgical, LLC,FDA registration: United States Class I

None GUDID I

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