Aesculap
by Aesculap AG Germany EUDAMEDGUDID
Ref DP726R
Product code DZNEMDN V030201
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number40392390000005852S | Date19 Jan 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04038653149070 | Date20 May 2020 | StatusIn distribution |
Coverage
- Active
- Listed
- Not covered
- European Union
- United States
Specification
- Generic Name
- General-purpose calliper, metallic
- Device Name
- Caliper Ir&m
- Model / Ref / Catalog
- DP726R
- Primary DI / UDI-DI
- 04038653149070
- Basic UDI-DI
- 40392390000005852S
- Direct Marketing DI
- 04038653149070
- FDA Product Code
- DZN
- EMDN Code
- V030201 Calipers
- GMDN Term
- General-purpose calliper, metallic
- Device Class
- Class I
- Regulation Number
- 872.4565
- Market of Registration
- Germany
- Commercial Distribution
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Manufacturer details
- EUDAMED SRN
- DE-MF-000005504
Other devices from Aesculap AG
Properties & raw data
Show properties, registry sources and raw records
Other properties (19)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Expiration Date: No
- Manufacturing Date: No
Sources (2)
- EUDAMED 897a14d6-dd58-4e67-84f3-6f8467a670f6
- FDA UDI e6f091f4-74c7-4301-868a-f2e290914075