Identity
- Trade Name
- Gimmi FDA UDI
- Generic Name
- Uterine probe FDA UDI
- Device Name
- SIMS UTERINE SOUND MALLEABLE, GRADUATED IN CM LENGTH 320 MM FDA UDI
- Model / Reference
- GQ.1587.32 FDA UDI
- Description
- SIMS UTERINE SOUND MALLEABLE, GRADUATED IN CM LENGTH 320 MM FDA UDI
Identifiers
- Catalog Number
- GQ.1587.32 FDA UDI
- Primary DI / UDI-DI
- 04049047045267 FDA UDI
- FDA Product Code
- HHM FDA UDI
- GMDN Term
- Uterine probe FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 884.4530 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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: Uterine probe
Gimmi by Gimmi GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Uterine probe.
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- GEN2 — SURGIX MEDICAL LLC · Class II
- BR Surgical, LLC — BR SURGICAL LLC · Class I
- Vaginal Probe — CooperSurgical, Inc. · Class I
- V. Mueller — STERIS CORPORATION · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Gimmi GmbH
Sources (1)
- FDA UDI 8a9e5a30-ea18-442b-bbf7-126f1c49c956 35 fields · synced May 30, 2026