Identity
- Trade Name
- Gimmi FDA UDI
- Generic Name
- Rib/sternum binder, reusable FDA UDI
- Device Name
- Surgical Instrument EUDAMEDCHEST-SUPPORT WITH SUPPORT-ROD AND JOINT COMPLETE, FOR ADULTS LENGTH 340 MM FDA UDI
- Model / Reference
- QL.3008.01 EUDAMEDFDA UDI
- Description
- CHEST-SUPPORT WITH SUPPORT-ROD AND JOINT COMPLETE, FOR ADULTS LENGTH 340 MM FDA UDI
Identifiers
- Catalog Number
- QL.3008.01 FDA UDI
- Primary DI / UDI-DI
- 04049047224747 EUDAMEDFDA UDI
- Basic UDI-DI
- 4049047LFH03ANA27DROL4 EUDAMED
- Direct Marketing DI
- 04049047224747 EUDAMED
- FDA Product Code
- CCW FDA UDI
- EMDN Code
- L99 SURGICAL INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Rib/sternum binder, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 868.5540 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Category: Rib/sternum binder, reusable
Gimmi by Gimmi GmbH — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Unknown
MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | MDR | — | Class I | Unknown |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Gimmi GmbH
Sources (2)
- FDA UDI 3a660e1a-04c3-4887-906a-5383e8d99ef2 35 fields · synced Jun 19, 2026
- EUDAMED 39ce0c90-9065-4afe-804d-2bfe9aa45c32 61 fields · synced Jun 14, 2026