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Aesculap, product family

by Aesculap AGand 1 other manufacturer record 8 variants Basic UDI-DI 403923900000070022

Shared by every variant

Manufacturer
Aesculap AG(6)AESCULAP, INC.(2)
Several manufacturer records share this Basic UDI-DI.
Basic UDI-DI
403923900000070022
Risk class
Class I
Legislation
MDR
EMDN category
NEEDLES AND APPLICATORS FOR LIGATURES, REUSABLE
Market status
8 on the market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 403923900000070022.

Recalls

0 recalls · FDA

No recall matched the devices on this page.

Recalls matched to the 8 devices listed on this page; other pages of the family can carry others.

Variants

8 devices · page 1 of 1

Variants of Aesculap, Basic UDI-DI 403923900000070022
UDI-DISize and differences
Aesculap
Aesculap AG
BM711R04038653140060 —On the market
Aesculap
Aesculap AG
BM712R04038653140077 —On the market
Aesculap
Aesculap AG
BM713R04038653140084 —On the market
Aesculap
Aesculap AG
BM714R04038653140091 —On the market
Aesculap
Aesculap AG
BM728R04038653140121 —On the market
Aesculap
Aesculap AG
BM729R04038653140138 —On the market
AESCULAP BM726R
AESCULAP, INC.
BM726R / BM726R04038653140107 —On the market
AESCULAP BM727R
AESCULAP, INC.
BM727R / BM727R04038653140114 —On the market