Identity
- Trade Name
- CRYOPETTE FDA UDI
- Generic Name
- Assisted reproduction vitrification carrier FDA UDI
- Device Name
- CRYOPETTE FDA UDI
- Model / Reference
- CRY-PETTE-BLACK FDA UDI
- Description
- CRYOPETTE FDA UDI
Identifiers
- Primary DI / UDI-DI
- 20888937900068 FDA UDI
- FDA Product Code
- MQK FDA UDI
- GMDN Term
- Assisted reproduction vitrification carrier 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
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
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: Assisted reproduction vitrification carrier
Cryopette by Origio Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Assisted reproduction vitrification carrier.
- S-CRYOLOCK (B) — BIOTECH INCORPORATED · Class II
- VitriGuard — Origio A/S · Class II
- Serological Pipette 1 mL — BIRR Biosciences BV · Class IIa
- Dry Incubator / EC6S-230MR — ASTEC CO.,Ltd · Class IIa
- Kryo 500 Series Controlled Rate Freezer — PLANER LIMITED · Class I
- VitriGuard — Origio A/S · Class II
- S-CRYOLOCK (G) — BIOTECH INCORPORATED · Class II
- iDAScore — Vitrolife A/S · 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 II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Origio Inc.
Sources (1)
- FDA UDI 0c2aa57c-e368-4701-91df-adb6ec9acba7 34 fields · synced Jun 1, 2026