Identity
- Trade Name
- G-Vitri™ Vitrification Straw FDA UDI
- Generic Name
- Tissue cryostorage straw FDA UDI
- Model / Reference
- SC-C-B FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06976438303256 FDA UDI
- 510(k) Number
- K240002 FDA UDI
- FDA Product Code
- MQK FDA UDI
- GMDN Term
- Tissue cryostorage straw FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.6160 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Tissue cryostorage straw
G-Vitri™ Vitrification Straw by Gimbo Medical Technology Shenzhen Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Tissue cryostorage straw.
- Cryotec — REPROLIFE INC. · Class II
- Vitri Plate — REPROLIFE INC. · Class II
- Cryotec — REPROLIFE INC. · Class II
- Cryotec — REPROLIFE INC. · Class II
- Cryotec — REPROLIFE INC. · Class II
- Warm Plate — REPROLIFE INC. · Class II
- Cryotec — REPROLIFE INC. · Class II
- Cryotec — REPROLIFE INC. · Class II
Cleared under the same submission
K240002 also covers:
- G-Vitri™ Vitrification Straw — Gimbo Medical Technology Shenzhen Co., Ltd.
- G-Vitri™ Vitrification Straw — Gimbo Medical Technology Shenzhen Co., Ltd.
- G-Vitri™ Vitrification Straw — Gimbo Medical Technology Shenzhen Co., Ltd.
- G-Vitri™ Vitrification Straw — Gimbo Medical Technology Shenzhen Co., Ltd.
- G-Vitri™ Vitrification Straw — Gimbo Medical Technology Shenzhen Co., Ltd.
- G-Vitri™ Vitrification Straw — Gimbo Medical Technology Shenzhen Co., Ltd.
- G-Vitri™ Vitrification Straw — Gimbo Medical Technology Shenzhen Co., Ltd.
- G-Vitri™ Vitrification Straw — Gimbo Medical Technology Shenzhen Co., Ltd.
- G-Vitri™ Vitrification Straw — Gimbo Medical Technology Shenzhen Co., Ltd.
- G-Vitri™ Vitrification Straw — Gimbo Medical Technology Shenzhen Co., Ltd.
- G-Vitri™ Vitrification Straw — Gimbo Medical Technology Shenzhen Co., Ltd.
- G-Vitri™ Vitrification Straw — Gimbo Medical Technology Shenzhen Co., Ltd.
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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Gimbo Medical Technology Shenzhen Co., Ltd.
Sources (1)
- FDA UDI 0640c0e4-602f-4a6d-98a6-801d8d5235d5 33 fields · synced Jun 8, 2026