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Aesculap, product family

by Aesculap AGand 1 other manufacturer record 9 variants Basic UDI-DI 40392390000004482F

Shared by every variant

Manufacturer
Aesculap AG(8)AESCULAP, INC.(1)
Several manufacturer records share this Basic UDI-DI.
Basic UDI-DI
40392390000004482F
Risk class
Class I
Legislation
MDR
EMDN category
SPREADERS AND RETRACTORS FOR GENERAL SURGERY, REUSABLE - OTHER
Market status
9 on the market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 40392390000004482F.

Recalls

0 recalls · FDA

No recall matched the devices on this page.

Recalls matched to the 9 devices listed on this page; other pages of the family can carry others.

Variants

9 devices · page 1 of 1

Variants of Aesculap, Basic UDI-DI 40392390000004482F
UDI-DISize and differences
Aesculap
Aesculap AG
BV825R04038653145003 —On the market
Aesculap
Aesculap AG
BV826R04038653145010 —On the market
Aesculap
Aesculap AG
BV828R04038653145034 —On the market
Aesculap
Aesculap AG
BV833R04038653272143 —On the market
Aesculap
Aesculap AG
BV834R04038653261345 —On the market
Aesculap
Aesculap AG
BV835R04038653145065 —On the market
Aesculap
Aesculap AG
BV839R04038653261369 —On the market
Aesculap
Aesculap AG
BV840R04038653262502 —On the market
AESCULAP BV827R
AESCULAP, INC.
BV827R / BV827R04038653145027 —On the market