Identity
- Trade Name
- Gimmi FDA UDI
- Generic Name
- Sphincteroscope FDA UDI
- Device Name
- Surgical Instrument EUDAMEDHIRSCHMANN ANUSCOPE FIG. 1 Ø 16 MM X 60 MM FDA UDI
- Model / Reference
- PU.1632.01 EUDAMEDFDA UDI
- Description
- HIRSCHMANN ANUSCOPE FIG. 1 Ø 16 MM X 60 MM FDA UDI
Identifiers
- Catalog Number
- PU.1632.01 FDA UDI
- Primary DI / UDI-DI
- 04049047317005 EUDAMEDFDA UDI
- Basic UDI-DI
- 4049047LBJ03ANA27DROHE EUDAMED
- Direct Marketing DI
- 04049047317005 EUDAMED
- FDA Product Code
- FFO FDA UDI
- EMDN Code
- L0406 RIGID RECTOSCOPES AND ANOSCOPES, REUSABLE EUDAMED
- GMDN Term
- Sphincteroscope FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 876.4730 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: Sphincteroscope
Gimmi by Gimmi GmbH — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS
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Also classified as Sphincteroscope.
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- THD L-PROCTO (TR/NS) — THD S.P.A. · Class I
- proctoscopes — HILBRO INSTRUMENTS (PVT) LTD · Class I
- Surgical Instrument — GIMMI GMBH · Class I
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 9e587393-2db2-44a2-a031-31a7746fe594 35 fields · synced Jul 8, 2026
- EUDAMED e82d1203-10a6-4cbe-a1c3-6d906eaaf8b3 61 fields · synced Jun 18, 2026